首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 62 毫秒
1.
Pressure-induced phase transformation of orthoenstatite to clinoenstatite has been studied at 7–10 GPa using a multi-anvil high pressure device with low stress (< 10MPa) conditions. At 1000 °C clinoenstatite was stabilized at pressures above 7.5 GPa. The obtained phase boundary is consistent with natural observations and previous experimental studies performed under quasi-hydrostatic condition, suggesting that clinoenstatite is a stable high pressure phase. Large differences in dP/dT slope between this result and those of earlier studies performed with piston cylinder and belt apparatus may be attributed to large differential stress in the high pressure cells of latter studies. The present study suggests that clinoenstatite can be stabilized by either hydrostatic pressure or differential stress and that the latter tends to shift the transformation boundary defined under hydrostatic condition to lower pressure.  相似文献   

2.
Polycrystalline ruby (α-Al2O3:Cr3+), a widely used pressure calibrant in high-pressure experiments, was compressed to 68.1 GPa at room temperature under non-hydrostatic conditions in a diamond anvil cell. Angle-dispersive X-ray diffraction experiments in a radial geometry were conducted at beamline X17C of the National Synchrotron Light Source. The stress state of ruby at high pressure and room temperature was analyzed based on the measured lattice strain. The differential stress of ruby increases with pressure from ~3.4 % of the shear modulus at 18.5 GPa to ~6.5 % at 68.1 GPa. The polycrystalline ruby sample can support a maximum differential stress of ~16 GPa at 68.1 GPa under non-hydrostatic compression. The results of this study provide a better understanding of the mechanical properties of this important material for high-pressure science. From a synthesis of existing data for strong ceramic materials, we find that the high-pressure yield strength correlates well with the ambient pressure Vickers hardness.  相似文献   

3.
Single crystals of α-quartz and α-berlinite AlPO4 have been compressed at high pressure and room temperature in a diamond anvil cell (DAC). The pressure-induced microstructures have been studied on recovered specimens using transmission electron microscopy. As previously reported, quartz is shown to exhibit an amorphous transition at high pressure (≈30 GPa). Under the markedly non-hydrostatic conditions of the present study, a wide mixed-phase regime in which amorphous lamellae form within the crystalline matrix is encountered at lower values of the mean stress. The amorphous lamellae are interpreted as shear lamellae. The formation of these shear lamellae as well as their habit planes are described by the evolution with pressure of shear moduli μ as computed in anisotropic elasticity. Our calculations also show instabilities at higher pressure of the elastic moduli (i.e. of the α-quartz structure) which are related to the amorphous transition. Berlinite exhibits a more ductile behavior with simultaneous dislocation activity and shear on amorphous lamellae which become pervasive at high pressure (≈10 GPa). These amorphous lamellae of berlinite do not revert to crystal when pressure is released.  相似文献   

4.
Residual pressure around mineral inclusions in diamond can provide useful information on the depth of diamond origin. Differential stress between an inclusion and host diamond arises from differences in thermal expansion and compressibility between host diamond and minerals. We determined residual pressure around mineral inclusions in a diamond from the Internationalnaya pipe, Yakutia, Russia, using the three-dimensional Raman mapping system developed recently by our group. The maximum residual pressures around the olivine and chromite inclusions were determined to be 0.69 GPa and 0.75 GPa, respectively. We proposed an advanced method for determining simultaneously pressure and temperature conditions where the mineral inclusions were trapped in the host diamond. The obtained values were 3.0 GPa and 447 °C, but these values are lower than typical P-T conditions in the mantle. Several technical possibilities for the discrepancy are discussed.  相似文献   

5.
ABSTRACT

The preservation of metastable diamond in ultrahigh-pressure metamorphic (UHPM) complexes challenges our understanding of the processes taking place during exhumation of these subduction zone complexes. The presence of diamonds in UHPM rocks implies that diamonds remained metastable during exhumation, and within thermodynamic stability of graphite for an extended period. This work studies the influence of pressure on the surface graphitization rate of diamond monocrystals in carbonate systems to understand the preservation of microdiamond during exhumation of UHP subduction complexes. Experiments were performed with 2–3 mm synthetic diamond monocrystals at 2–4 GPa in СаСО3 (1550°С) and К2СО3 (1450°С) melts using a high-pressure multi-anvil apparatus. The highest rate of surface graphitization took place at 2 GPa; diamond crystals were almost completely enveloped by a graphite coating. At 4 GPa, only octahedron-shaped pits formed on flat {111} diamond crystal faces. Our results demonstrate that the surface graphitization rate of diamonds in the presence of carbonate melts at 1450–1550°C increases with decreasing pressure. Decreased pressure alone can graphitize diamond regardless of exhumation rate. Metastable diamond inclusions survive exhumation with little or no graphitization because of excess pressure up to 2 GPa acting on them, and because inclusions are protected from interaction with C-O-H fluid.  相似文献   

6.
Single-crystal brucite, Mg(OH)2, was studied to 14 GPa in a quasi-hydrostatic pressure medium using a diamond anvil cell and energy-dispersive synchrotron x-ray diffraction. The parameters of a third-order Birch-Murnaghan equation of state fit to the data are: K OT=42(2) GPa, and (?K OT/?P)T= 5.7(5). The bulk modulus is significantly lower than that obtained in recent shock compression and powder x-ray diffraction experiments under non-hydrostatic conditions. No evidence was found for a transition involving the Mg -O sub-structure over the pressure range of these experiments. This implies that the structural change previously identified at high pressure by Raman spectroscopy probably involves rearrangement of hydrogen atoms, leaving the Mg — O substructure largely unaffected.  相似文献   

7.
Precise determination of the partitioning of Mg and Fe2+ between olivine and ultramafic melt has been made at pressures from 5 to 13 GPa using a MA-8 type multi-anvil high-pressure apparatus (PREM) installed at Earthquake Research Institute, University of Tokyo. A very short rhenium capsule (<100 μm sample thickness) was adopted to minimize temperature variation within the sample container. Synthetic gels with the composition of the upper mantle peridotite were used as starting materials to promote the homogeneity. Analyses of quenched melts and coexisting olivines were made with an electron probe microanalyzer. The obtained partition coefficient, KD [=(FeO/MgO)ol/(FeO/MgO)melt], decreases from 0.35 to 0.25 with increasing pressure from 5 to 13 GPa, suggesting a negative correlation between pressure and KD above 5 GPa. Our result is consistent with a parabolic relationship between KD and degree of polymerization (NBO/T) of melts reported by previous studies at lower pressures. The negative correlation between pressure and KD suggests that olivine crystallizing in a magma ocean becomes more Mg-rich with depth and that primary magmas generated in the upper mantle become more Fe-rich with depth than previously estimated.  相似文献   

8.
Studies of mass transport and kinetics in minerals at high pressure often require a sample environment in which the stress is near-hydrostatic and the chemical environment is carefully controlled. We report here details of a multianvil sample assembly in which these requirements are fulfilled and which has been used to study the effect of pressure on the kinetics of dislocation recovery in olivine up to 10 GPa. Annealing experiments have been performed on single crystals of San Carlos olivine at 8.5 GPa and 1400° C in a 1200 tonne split-sphere multianvil apparatus. The sample assembly consists of an 18 mm MgO octahedron with a LaCrO3 heater of variable wall thickness to give a small temperature variation (20° C) along the 3 mm length of the sample capsule. To minimize the differential stress on the sample, the olivine single crystal is surrounded by NaCl and both pressurization and depressurization are performed slowly at a temperature of 600° C (to minimize the strength of the NaCl). The silica activity is buffered by orthopyroxene powder in contact with the olivine and the oxygen fugacity is buffered by Ni + NiO within the sample capsule. The H2O-content of the sample assembly is minimized by drying all components at 230° C under vacuum. Olivine single crystals recovered after annealing at 1400° C and 8.5 GPa show no evidence of deformation, either ductile or brittle. Dislocation densities of 109–1010 m-2 are similar to those observed prior to high-pressure annealing and indicate differential stresses of <10 mpa.=" infrared=" spectroscopy=" indicates=" that=" the=" hydrogen=" content=" of=" a=" sample=" annealed=" at=" 10=" gpa,=" 1500°=" c=" for=" 21=" h=" is=">13 H/106Si, which, although low, is higher than that of the crystals prior to high-pressure annealing. Finally, the effectiveness of the fO2 buffer has been verified by estimating the fO2 at the surface of the sample from the solubility of Fe in Pt metal in equilibrium with the olivine and orthopyroxene.  相似文献   

9.
We used an in situ measurement method to investigate the phase transition of Fe2SiO4 polymorphs under high pressures and temperatures. A multi-anvil high-pressure apparatus combined with synchrotron X-ray radiation was used. The stability of each polymorph was identified by observing the X-ray diffraction data from the sample. In most experiments, the diffraction patterns were collected 10–30 min after reaching the desired pressure and temperature conditions. The transition boundary between the olivine and spinel phase at T = 1,000–1,500 K and P = 2–8 GPa was determined to occur at P (GPa) = 0.5 + 0.0034 × T (K). The transition pressure determined in this study was in general agreement with that observed in previous high-pressure experiments. However, the slope of the transition, dP/dT, determined in our study was significantly higher than that estimated by the previous study combined with the in situ X-ray method.  相似文献   

10.
Raman spectra of Mg2GeO4-olivine were obtained from ambient pressure up to 34 GPa at ambient temperature. Under quasi-hydrostatic pressure conditions, the following modifications in the Raman spectra occur as pressure increases: 1) near 11 GPa, two sharp extra bands appear in the 600–700 cm?1 frequency range, and increase in intensity with respect to the olivine bands; 2) above 22 GPa, these two bands become very intense, and the number, position and relative intensity of the other vibrational bands drastically change; 3) the intensity of sharp bands progressively decreases above 25 GPa. The transformation occurs at lower pressures under non-hydrostatic conditions. During decompression to atmospheric pressure, the high-pressure phase partially reverts to olivine. These observations can be interpreted as the progressive metastable transformation from the olivine structure to a crystalline phase with four-fold coordinated Ge, in which the GeO4 tetrahedra are polymerized. We propose that the metastable high-pressure phase is a structurally disordered spinelloid close to the hypothethical ω- or ?*-phase, and forms by a shear mechanism assisted by the development of a dynamical instability in the olivine structure. Implications for the transformations undergone by olivines under far-from-equilibrium conditions (e.g. in subducting lithospheric slabs and in shocks) are discussed.  相似文献   

11.
The deviatoric stress produced in a large-volume, high-pressure apparatus of the girdle-anvil type has been estimated from the density of free dislocations induced in natural olivine single crystals (initial density of 2×106 cm?2). Experiments at maximum pressure P=40 kbar and temperature T=1050°C for t=1 h in NaCl cell assemblies and various P-T paths yield specimens whose dislocation densities are unchanged from this initial value, implying that the deviatoric stress was less than 140 bar. In BN cell assemblies, the recovered specimen from high P-T experiments exhibit much higher densities of dislocations (～109 cm?2) which have been produced by steady-state plastic deformation of the olivine crystals under a deviatoric stress of ～3 kbar. This value of deviatoric stress in BN has been corroborated by observations of the subgrain size and recrystallized grain size in specimens of longer run duration (3 h).  相似文献   

12.
石英高压相变研究进展   总被引：2，自引：0，他引：2  
罗扬  施旭  贺红亮  赵永红 《地学前缘》2007,14(3):149-157
文中总结了前人有关石英高温高压相变的实验结果。根据以前的实验,在静水压条件下,石英-柯石英-斯石英-CaCl2结构超斯石英相-α-PbO2结构超斯石英相之间的相变方程分别是:p(GPa)=(2.11±0.03)+(9.8×10-4±1.2×10-4)×T(℃),p(GPa)=(8.0±0.2)+(1.1×10-3±3×10-4)×T(℃),p(GPa)=(51±2)+(0.012±0.005)×T(K),p(GPa)=98+(0.0095±0.0016)×T(K)。文中还初步探讨了非静水压状态对石英相变的影响。实验结果表明,差应力的出现降低了石英相变所需要的围压,即相变边界向低压方向偏移,在周永胜等人实验数据的基础上,笔者尝试将二维的相图扩展到三维相图以考虑差应力的影响。最后讨论了石英相变在地学研究中的作用,对比不同的观点分析了前人对超高压变质作用过程的解释,希望可以为以后解释地质资料提供较为广泛的可能性,促进我们对地球内部动力学过程的了解。  相似文献   

13.
Single crystalline San Carlos olivine (1 mm cube) was transformed to (Mg,Fe)2SiO4β-phase at 13.5–15 GPa, 1030–1330 °C for 0–600 min using a multi-anvil high pressure apparatus. The α-β transformation occurred by incoherent surface nucleation and interface-controlled growth and recovered partially transformed samples showed sharply defined reaction rim. The growth rate of the β-phase rim significantly decreased with time and the growth eventually ceased. TEM observations revealed that many dislocations were created in both the relict olivine just near the α-β interface and the β-phase in the rim, which show evidence for deformation caused by interfacial stresses associated with the misfit elastic strain of the transformation. The observed tangled dislocation texture in β-phase suggested that the β-phase rim was hardened and relaxation of the interfacial stress was retarded. This probably caused a localized pressure drop in the relict olivine and decreased the growth rate. Time-dependent growth rates of β-phase is possibly controlled by the rheology of β-phase, which must be considered for the prediction of the olivine metastability in the subducting slabs. Received: 24 January 1997 / Revised, accepted: 24 July 1998  相似文献   

14.
Element partitioning between olivine and silicate melt has been investigated at pressures 1–14 GPa, by using a 6–8 type multi-anvil high pressure apparatus. In order to observe systematics in the partitioning of trivalent ions, Li was added to the starting materials in order to increase the concentration of trivalent ions in olivine. With increasing pressure, it was found that partition coefficients of most of the elements gradually decreased. Trivalent ions generally showed parabolic pattern on partition coefficient — ionic radius diagram. When pyrolite-like material was used as the starting material, partition coefficient of Al, DAl, gradually increased with increase in pressure while the partition coefficients of the other elements decreased, and the DAl deviated from the parabolic pattern of other trivalent ions. The deviation of DAl from the D pattern of the other trivalent ions was also found when olivine was employed as main component of the starting material. This result may be ascribed to the compositional change of coexisting silicate melt with increase in pressure.  相似文献   

15.
Experiments with peridotite minerals in simple (MgO–Al2O3–SiO2,CaO–MgO–SiO2 and CaO–MgO–Al2O3–SiO2)and natural systems were conducted at 1300–1500°Cand 6–10 GPa using a multi-anvil apparatus. The experimentsin simple systems demonstrated consistency with previous lowerpressure experiments in belt and piston–cylinder set-ups.The analysis of spatial variations in pyroxene compositionswithin experimental samples was used to demonstrate that pressureand temperature variations within the samples were less than0·4 GPa and 50°C. Olivine capsules were used in natural-systemexperiments with two mineral mixtures: SC1 (olivine + high-Alorthopyroxene + high-Al clinopyroxene + spinel) and J4 (olivine+ low-Al orthopyroxene + low-Al clinopyroxene + garnet). Theexperiments produced olivine + orthopyroxene + garnet ±clinopyroxene assemblages, occasionally with magnesite and carbonate-richmelt. Equilibrium compositions were derived by the analysisof grain rims and evaluation of mineral zoning. They were comparedwith our previous experiments with the same starting mixturesat 2·8–6·0 GPa and the results from simplesystems. The compositions of minerals from experiments withnatural mixtures show smooth pressure and temperature dependencesup to a pressure of 8 GPa. The experiments at 9 and 10 GPa producedandradite-rich garnets and pyroxene compositions deviating fromthe trends defined by the lower pressure experiments (e.g. higherAl in orthopyroxene and Ca in clinopyroxene). This discrepancyis attributed to a higher degree of oxidation in the high-pressureexperiments and an orthopyroxene–high-P clinopyroxenephase transition at 9 GPa. Based on new and previous resultsin simple and natural systems, a new version of the Al-in-orthopyroxenebarometer is presented. The new barometer adequately reproducesexperimental pressures up to 8 GPa. KEY WORDS: garnet; mineral equilibrium; multi-anvil apparatus; orthopyroxene; geobarometry  相似文献   

16.
This report considers experimental studies of the gravitation fractionating of xenocrysts (diamond, garnet, and olivine) in kimberlite magma at 4.0 GPa and 1400°C. The values obtained (0.6–0.7 m/h for 0.3-mm diamond crystals, 0.36 m/h for garnet grains, and 0.6–0.29 m/h for olivine grains) point to a high rate of xenocryst sinking in the ultralow-viscous kimberlite magma (as high as 1 m/h and more, depending on the densities and grain sizes of minerals). A high rate of xenocryst sinking in kimberlite magma results in the impossibility of preservation of heterogeneity in these melts for a sufficiently long time.  相似文献   

17.
We present a Raman spectroscopic study of the structural modifications of several olivines at high pressures and ambient temperature. At high pressures, the following modifications in the Raman spectra are observed: 1)?in Mn2GeO4, between 6.7 and 8.6?GPa the appearance of weak bands at 560 and 860?cm?1; between 10.6 and 23?GPa, the progressive replacement of the olivine spectrum by the spectrum of a crystalline high pressure phase; upon decompression, the inverse sequence of transformations is observed with some hysteresis in the transformation pressures; this sequence may be interpreted as the progressive transformation of the olivine to a spinelloid where Ge tetrahedra are polymerized, and then to a partially inverse spinel; 2)?in Ca2SiO4, the olivine transforms to larnite between 1.9 and 2.1?GPa; larnite is observed up to the maximum pressure of 24?GPa and it can partially back-transform to olivine during decompression; 3)?in Ca2GeO4, the olivine transforms to a new structure between 6.8 and 8?GPa; the vibrational frequencies of the new phase suggest that the phase transition involves an increase of the Ca coordination number and that Ge tetrahedra are isolated; this high pressure phase is observed up to the maximum pressure of 11?GPa; during decompression, it transforms to a disordered phase below 5?GPa; 4)?in CaMgGeO4, no significant modification of the olivine spectrum is observed up to 15?GPa; between 16 and 26?GPa, broadening of some peaks and the appearance of a weak broad feature at 700–900?cm?1 suggests a progressive amorphization of the structure; near 27?GPa, amorphization is complete and an amorphous phase is quenched down to ambient pressure; this unique behaviour is interpreted as the result of the incompatibilities in the high pressure behaviour of the Ca and Mg sublattices in the olivine structure.  相似文献   

18.
Effect of water and stress on the lattice-preferred orientation of olivine   总被引：6，自引：1，他引：5  
The influence of water and stress on the lattice-preferred orientation (LPO) of olivine aggregates was investigated through large strain, shear deformation experiments at high pressures and temperatures (P = 0.5–2.1 GPa, T = 1470–1570 K) under both water-poor and water-rich conditions. The specimens are hot-pressed synthetic olivine aggregates or single crystals of olivine. Water was supplied to the sample by decomposition of a mixture of talc and brucite. Deformation experiments were conducted up to γ (shear strain)  6 using the Griggs apparatus where water fugacity was up to  13 GPa at the pressure of 2 GPa. The water content in olivine saturated with water increases with increasing pressure and the solubility of water in olivine at P = 0.5–2 GPa was  400–1200 ppm H/Si. Several new types of LPO in olivine are found depending on water content and stress. Samples deformed in water-poor conditions show a conventional LPO of olivine where the olivine [100] axis is subparallel to the shear direction, the (010) plane subparallel to the shear plane (type-A). However, we identified three new types (type-B, C, and E) of LPO of olivine depending on the water content and stress. The type-B LPO of olivine which was found at relatively high stress and/or under moderate to high water content conditions is characterized by the olivine [001] axis subparallel to the shear direction, the (010) plane subparallel to the shear plane. The type-C LPO which was found at low stress and under water-rich conditions is characterized by the olivine [001] axis subparallel to the shear direction, the (100) plane subparallel to the shear plane. The type-E LPO which was found under low stress and moderate water content is characterized by the olivine [100] axis subparallel to the shear direction, the (001) plane subparallel to the shear plane. Observations by transmission electron microscopy (TEM) and scanning electron microscopy (SEM) show that the dislocations in water-poor samples (type-A) are curved and both b =  [100] and b = [001] dislocations have a similar population. Numerous subgrains are seen in water-poor samples in backscattered electron images. In contrast, water-rich samples (both type-B and type-C) contain mostly b = [001] dislocations and dislocations are straight and sub-grain boundaries are rare compared to those in water-poor samples. These observations suggest that (1) dominant slip systems in olivine change with water fugacity (and stress) and (2) grain boundary migration is enhanced in the presence of water. Seismic anisotropy corresponding to the fabrics under water-rich condition is significantly different from that under water-poor condition. Consequently, the relationship between seismic anisotropy and flow geometry in water-rich regions is expected to be different from that in water-poor regions in which type-A fabric dominates (i.e., the lithosphere). A few cases are discussed including anisotropy in the subduction zone and in the deep upper mantle.  相似文献   

19.
In situ strength measurements on natural upper-mantle minerals   总被引：1，自引：0，他引：1  
Using in situ strength measurements at pressures up to 10 GPa and at room temperature, 400, 600, and 700°C, we examined rheological properties of olivine, orthopyroxene, and chromian-spinel contained in a mantle-derived xenolith. Mineral strengths were estimated using widths of X-ray diffraction peaks as a function of pressure, temperature, and time. Differential stresses of all minerals increase with increasing pressure, but they decrease with increasing temperature because of elastic strain on compression and stress relaxation during heating. During compression at room temperature, all minerals deform plastically at differential stress of 4–6 GPa. During subsequent heating, thermally induced yielding is observed in olivine at 600°C. Neither orthopyroxene nor spinel shows complete stress relaxation, but both retain some stress even at 700°C. The strength of the minerals decreases in the order of chromian-spinel ≈ orthopyroxene > olivine for these conditions. This order of strength is consistent with the residual pressure of fluid inclusions in mantle xenoliths.  相似文献   

20.
We established an equation of state for nanocrystalline forsterite using multi-anvil press and diamond anvil cell. Comparative high-pressure and high-temperature experiments have been performed up to 9.6 GPa and 1,300°C. We found that nanocrystalline forsterite is more compressible than macro-powder forsterite. The bulk modulus of nanocrystalline forsterite is equal to 123.3 (±3.4) GPa whereas the bulk modulus of macro-powder forsterite is equal to 129.6 (±3.2) GPa. This difference is attributed to a weakening of the elastic properties of grain boundary and triple junction and their significant contribution in nanocrystalline sample compare to the bulk counterpart. The bulk modulus at zero pressure of forsterite grain boundary was determined to be 83.5 GPa.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号