排序方式： 共有137条查询结果，搜索用时 15 毫秒
81.
Régine?Mosser-RuckEmail author Isabella?Pignatelli Franck?Bourdelle Mustapha?Abdelmoula Odile?Barres Damien?Guillaume Delphine?Charpentier Davy?Rousset Michel?Cathelineau Nicolas?Michau 《Contributions to Mineralogy and Petrology》2016,171(11):97
The smectite-to-chlorite conversion is investigated through long-duration experiments (up to 9 years) conducted at 300 °C. The starting products were the Wyoming bentonite MX80 (79 % smectite), metallic iron and magnetite in contact with a Na–Ca chloride solution. The predominant minerals in the run products were an iron-rich chlorite (chamosite like) and interstratified clays interpreted to be chlorite/smectite and/or corrensite/smectite, accompanied by euhedral crystals of quartz, albite and zeolite. The formation of pure corrensite was not observed in the long-duration experiments. The conversion of smectite into chlorite over time appears to take place in several steps and through several successive mechanisms: a solid-state transformation, significant dissolution of the smectite and direct precipitation from the solution, which is over-saturated with respect to chlorite, allowing the formation of a chamosite-like mineral. The reaction mechanisms are confirmed by X-ray patterns and data obtained on the experimental solutions (pH, contents of Si, Mg, Na and Ca). Because of the availability of some nutrients in the solution, total dissolution of the starting smectite does not lead to 100 % crystallization of chlorite but to a mixture of two dominant clays: chamosite and interstratified chlorite/smectite and/or corrensite/smectite poor in smectite. The role of Fe/(Fe + Mg) in the experimental medium is highlighted by chemical data obtained on newly formed clay particles alongside previously published data. The newly formed iron-rich chlorite has the same composition as that predicted by the geothermometer for diagenetic to low-grade metamorphic conditions, and the quartz + Fe-chlorite + albite experimental assemblage in the 9-year experiment is close to that fixed by water–rock equilibrium. 相似文献
82.
83.
Priscille Cuvillier Noël Chaumard Hugues Leroux Brigitte Zanda Roger H. Hewins Damien Jacob Bertrand Devouard 《Meteoritics & planetary science》2018,53(3):482-492
We conducted a transmission electron microscope study of the exsolution microstructures of Ca-rich pyroxenes in type I chondrules from the Paris CM and Renazzo CR carbonaceous chondrites in order to provide better constraints on the cooling history of type I chondrules. Our study shows a high variability of composition in the augite grains at a submicrometer scale, reflecting nonequilibrium crystallization. The microstructure is closely related to the local composition and is thus variable inside augite grains. For compositions inside the pyroxene miscibility gap, with a wollastonite (Wo) content typically below 40 mole%, the augite grains contain abundant exsolution lamellae on (001). For grain areas with composition close to Wo40, a modulated texture on (100) and (001) is the dominant microstructure, while areas with compositions higher than Wo40 do not show any exsolution microstructure development. To estimate the cooling rate, we used the spacing of the exsolution lamellae on (001), for which the growth is diffusion controlled and thus sensitive to the cooling rate. Despite the relatively homogeneous microstructures of augite grains with Wo < 35 mole%, our study of four chondrules suggests a range of cooling rates from ~10 to ~1000 °C h−1, within the temperature interval 1200–1350 °C. These cooling rates are comparable to those of type II chondrules, i.e., 1–1000 °C h−1. We conclude that the formation of type I and II chondrules in the proto-solar nebula was the result of a common mechanism. 相似文献
84.
Here we report on two separate ongoing, multi-year investigations on the dependence of the dissolution rate (R) of albite feldspar on fluid saturation state, as defined by the Gibbs free energy of reaction (ΔGr) for dissolution. The investigations are based on dissolution at pH 9.2, 150 °C and pH 3.3, 100 °C. Both studies reveal that the R–ΔGr relation is highly non-linear and sigmoidal. The kinetic data from the first study, being the most complete, can be fitted with a sigmoidal rate curve that is composed of two separate, parallel rate laws that represent distinct mechanisms of dissolution. The switch between one dominant mechanism and the other may be controlled by a critical free energy. The fact that in both studies the same type of sigmoidal R–ΔGr relation exists for dissolution at different pH and temperature condition suggests that this behavior may be universal for albite and other feldspars. Moreover, the experimental data contradict the commonly used R–ΔGr relation that is loosely based on transition state theory (TST). This has important implications with respect to the accuracy of geochemical codes that model water–rock interactions at near-equilibrium conditions. 相似文献
85.
In-Street Wind Direction Variability in the Vicinity of a Busy Intersection in Central London 总被引：3，自引：2，他引：1
Ahmed A. Balogun Alison S. Tomlin Curtis R. Wood Janet F. Barlow Stephen E. Belcher Robert J. Smalley Justin J. N. Lingard Sam J. Arnold Adrian Dobre Alan G. Robins Damien Martin Dudley E. Shallcross 《Boundary-Layer Meteorology》2010,136(3):489-513
We present results from fast-response wind measurements within and above a busy intersection between two street canyons (Marylebone Road and Gloucester Place) in Westminster, London taken as part of the DAPPLE (Dispersion of Air Pollution and Penetration into the Local Environment; www.dapple.org.uk ) 2007 field campaign. The data reported here were collected using ultrasonic anemometers on the roof-top of a building adjacent to the intersection and at two heights on a pair of lamp-posts on opposite sides of the intersection. Site characteristics, data analysis and the variation of intersection flow with the above-roof wind direction (θ ref ) are discussed. Evidence of both flow channelling and recirculation was identified within the canyon, only a few metres from the intersection for along-street and across-street roof-top winds respectively. Results also indicate that for oblique roof-top flows, the intersection flow is a complex combination of bifurcated channelled flows, recirculation and corner vortices. Asymmetries in local building geometry around the intersection and small changes in the background wind direction (changes in 15- min mean θ ref of 5°–10°) were also observed to have profound influences on the behaviour of intersection flow patterns. Consequently, short time-scale variability in the background flow direction can lead to highly scattered in-street mean flow angles masking the true multi-modal features of the flow and thus further complicating modelling challenges. 相似文献
86.
Abstract— Four particles extracted from track 80 at different penetration depths have been studied by analytical transmission electron microscopy (ATEM). Regardless of their positions within the track, the samples present a comparable microstructure made of a silica rich glassy matrix embedding a large number of small Fe‐Ni‐S inclusions and vesicles. This microstructure is typical of strongly thermally modified particles that were heated and melted during the hypervelocity impact into the aerogel. X‐ray intensity maps show that the particles were made of Mg‐rich silicates (typically 200 nm in diameter) cemented by a fine‐grained matrix enriched in iron sulfide. Bulk compositions of the four particles suggest that the captured dust particle was an aggregate of grains with various iron sulfide fraction and that no extending chemical mixing in the bulb occurred during the deceleration. The bulk S/Fe ratios of the four samples are close to CI and far from the chondritic meteorites from the asteroidal belt, suggesting that the studied particles are compatible with chondritic‐porous interplanetary dust particles or with material coming from a large heliocentric distance for escaping the S depletion. 相似文献
87.
The composition of carbonate minerals formed in past and present oceans is assumed to be significantly controlled by temperature and seawater composition. To determine if and how temperature is kinetically responsible for the amount of Mg incorporated in calcite, we quantified the influence of temperature and specific dissolved components on the complex mechanism of calcite precipitation in seawater. A kinetic study was carried out in artificial seawater and NaCl-CaCl2 solutions, each having a total ionic strength of 0.7 M. The constant addition technique was used to maintain [Ca2+] at 10.5 mmol kg−1 while [] was varied to isolate the role of this variable on the precipitation rate of calcite.Our results show that the overall reaction of calcite precipitation in both seawater and NaCl-CaCl2 solutions is dominated by the following reaction:
88.
Laurent Truche Gilles Berger Damien Guillaume 《Geochimica et cosmochimica acta》2010,74(10):2894-2914
The kinetics of abiotic redox reactions induced by hydrogen are poorly documented although it represents a growing area of interest in terms of both nuclear waste storage assessment and the comprehensive study of hydrogen-rich fluid in mid-ocean ridge hydrothermal systems. We present an experimental kinetics study of pyrite reduction into pyrrhotite under significant H2 pressure and mid-hydrothermal conditions. We describe the mechanism and kinetic behavior of this reaction by combining textural and solution analyses under various conditions of temperature, pyrite particles size, H2 pressure and pH. When pH is controlled by calcite, the reaction presents all the characteristics of a coupled dissolution-precipitation mechanism occurring at the pyrite-pyrrhotite interface. By considering the chemical affinity of the coupled reaction as a function of reaction extent, we demonstrate that the spatial coupling is induced both by pyrite as a substrate for pyrrhotite nucleation and by the role of fluid chemistry at the reaction front. Far from equilibrium with respect to pyrite, the kinetics of sulfide production associated with the reaction are linearly related to the square root of time with an activation energy of 53 kJ/mol. This value is higher than what is expected for a diffusion-controlled kinetic regime. We suggest that the reaction rate is controlled both by pyrite reductive dissolution and by sulfide diffusion through the porous pyrrhotite microstructure. We provide a simple sulfide production-rate expression on the basis of our measured rate constants that can be used in geochemical modeling to further evaluate the impact of hydrogen on pyrite under nuclear waste disposal conditions. 相似文献
89.
Geomorphologic evidence for Plio‐Quaternary shortening in the southern Neuquén basin (40°S,Argentina) 
下载免费PDF全文
下载免费PDF全文 A morphostructural analysis of a Pliocene flood basalt formation in the southern Neuquén basin (40°S) shows evidence of contractional deformation less than 3.5 Ma ago. This formation exhibits a general dip towards the south‐east, with relict outcrops located 100 m higher than the main source volcano, which suggests a local tilting of the lava flow. This tilt has been brought about by Plio‐Quaternary reactivation of the eastern border of the Sañico Massif along two thrusts that offset the lava flow. Another long‐wavelength bulge in the southern part of the lava flow unit indicates a possible Pliocene uplift of the North Patagonian Massif. These results provide new evidence of continuing shortening in the Neuquén basin during the Plio‐Quaternary, challenging the hypothesis that an extensional regime has existed since the end of the Miocene in this basin. 相似文献
90.
Haberkorn H Tran D Massabuau JC Ciret P Savar V Soudant P 《Marine pollution bulletin》2011,62(6):1191-1197
The complexity of the relationships between Alexandrium minutum (A.m.) concentration in the water ([A.m.]w), Paralytic Shellfish Poisoning contamination in the digestive gland ([PSP]dg) and valve behavior was explored in oysters Crassostrea gigas. Two experiments were conducted, during which oysters’ valve behaviour were analyzed. Oysters, first acclimated for 10-days with the non harmful microalgae Heterocapsa triquetra (H.t.), were exposed to four microalgae mixtures at constant total concentrations of 10 × 103 cells ml−1 (experiment-1) and 5 × 103 cells ml−1 (experiment-2): 100% A.m.; 50% A.m.-50% H.t.; 25% A.m.-75% H.t.; 100% H.t. At the end of experiment-2, [PSP]dg were measured.At 10 × 103 cells ml−1, the microalgal ingestion decreased (p < 0.05) with increasing [A.m.]w but not at 5 × 103 cells ml−1 (p > 0.05). The frequency of microclosures specifically increased with [A.m.]w (p < 0.05) and the opening duration with [PSP]dg (p < 0.0001). Oysters exhibiting the maximum increase in opening duration also exhibited the highest [PSP]dg. The results are discussed in terms of oyster physiology and origin of the behavioral response. 相似文献