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1.
27Al,29Si MAS NMR studies of kaolinite and its thermal transformation products show that in the kaolinite-mullite reaction series
there is an extensive segregation of Al2O3 and SiO2 and the reaction of Al2O3 with SiO2 to form mullite is the main path of mullite formation. At about 850° C, the peak intensity of A1(V) reaches its maximum and
with the further rise of temperature the A1(V) signal completely disappears. At about 950°C, γ-Al2O3 accounts for about 71% of the material phases containing Al atoms. In the series there is no obvious presence of Al-Si spinel.
The27Al and29Si MAS NMR spectra show that there is an obvious difference between the temperature points for Al-O2(OH)4 octahedral sheet collapsing and Si-O4 tetrahedral sheet breaking down. 相似文献
2.
The heat capacity and vibrational entropy of a calcium aluminate and three peraluminous calcium aluminosilicate glasses have been determined from 2 to 300 K by heat-pulse relaxation calorimetry. Together with previous adiabatic data for six other glasses in the system CaO-Al2O3-SiO2, these results have been used to determine partial molar heat capacities and entropies for five species namely, SiO2, CaO and three different sorts of Al2O3 in which Al is 4-, 5- and 6-fold coordinated by oxygen. Given the determining role of oxygen coordination on low-temperature heat capacity, the composition independent entropies found for SiO2 and CaO indicate that short-range order around Si and Ca is not sensitive to aluminum speciation up to the highest fraction of 25% observed for VAl by NMR spectroscopy. Because of the higher room-temperature vibrational entropy of IVAl2O3 (72.8 J/mol K) compared to VAl2O3 (48.5 J/mol K), temperature-induced changes from IVAl to VAl give rise to a small negative contribution of the order of 1 J/mol K to the partial molar configurational heat capacity of Al2O3 in melts. Near 0 K, pure SiO2 glass distinguishes itself by the importance of the calorimetric boson peak. On a g atom basis, the maximum of this peak varies with the composition of calcium aluminosilicate glasses by a factor of about 2. It does not show smooth variations, however, either as a function of SiO2 content, at constant CaO/Al2O3 ratio, or as a function of Al2O3 content, at constant SiO2 content. 相似文献
3.
We have experimentally studied the behavior of oxygen isotope composition in silicate melts with a wide range of network-forming cations. Isotopic equilibration of the Di-An eutectic melts modified by addition of Si, Al, Ti, and Fe was carried out in a vertical tube furnace within a temperature range from 1400 to 1570°C. It was established that the value 10 3Lnα between silicic and basic melts at 1400 and 1450°C systematically increases with increase of SiO2 content, reaching ≈1‰ at 20% melt silica enrichment. The effect of the Fe2O3, TiO2, and Al2O3 contents was studied at 1500°C. An increase in Fe2O3 from 5 to 20 wt % causes a 0.4‰ increase of δ18O. An increase in Ti and Al contents results in the non-linear behavior of δ18O, which decreases in the region of the highest TiO2 (28.4%) and Al2O3 (29.3 %) contents. In the region of moderate Fe2O3, TiO2, and Al2O3 contents, the values of δ18O show monotonous linear dependence on the oxide contents. Methods of estimations of oxygen isotope fractionation coefficients at T > 1400°C in the studied range of network-forming oxides are considered on the basis of experimental data. The calculation of fractionation coefficients with the use of I18O index showed that experimental values with increase of SiO2 content deviate from calculated values by 0.3‰ for basic melts and 0.5–0.6‰ in the region of silicic melts. Similar pattern is observed during approximation of a melt by normative mineral composition. The calculation with the Garlick index leads to the systematic underestimation (on average, by 0.3‰) of 103Lnα as compared to the experimental data. The NBO/T ratio appeared the best parameter to describe 103Lnα in the melt-melt system, including the region of high-Fe melts. Analysis of experimental data leads us to conclude that the degree of polymerization of the melts in the studied temperature-composition region is the most important factor affecting the oxygen-isotope fractionation in the melt-melt system. Empirical index similar to the Garlick index was proposed to take into account oxygen associated with T-cations: $$I^m = (C_{Si} + aC_{Al} + bC_{Ti} + cC_{Fe^{3 + } } )/\Sigma C_i ,$$ where a, b, and c constants are empirically established coefficients: 0.75, 0. 70, and 1.75, respectively. 相似文献
4.
We have investigated grain boundary diffusion rates in enstatite by heating single crystals of quartz packed in powdered San Carlos olivine (Mg0.90Fe0.10)2SiO4 at controlled oxygen fugacities in the range 10?5.7 to 10?8.7?atm and temperatures from 1350° to 1450?°C for times from 5 to 100?h at 1?atm total pressure. Following the experiments, the thickness of the coherent polycrystalline reaction rim of pyroxene that had formed between the quartz and olivine was measured using backscatter scanning imaging in the electron microprobe. Quantitative microprobe analysis indicated that the composition of this reaction phase is (Mg0.92Fe0.08)2Si2O6. The rate of growth of the pyroxene increases with increasing temperature, is independent of the oxygen fugacity, and is consistent with a parabolic rate law, indicating that the growth rate is controlled by ionic diffusion through the pyroxene rim. Microstructural observations and platinum marker experiments suggest that the reaction phase is formed at the olivine-pyroxene interface, and is therefore controlled by the diffusion of silicon and oxygen. The parabolic rate constants determined from the experiments were analyzed in terms of the oxide activity gradient across the rim to yield mean effective diffusivities for the rate-limiting ionic species, assuming bulk transport through the pyroxene layer. These effective diffusivities are faster than the lattice diffusivities for the slowest species (silicon) calculated from creep experiments, but slower than measured lattice diffusivities for oxygen in enstatite. Thus, silicon grain boundary diffusion is most likely to be the rate-limiting process in the growth of the pyroxene rims. Also, as oxygen transport through the pyroxene rims must be faster than silicon transport, diffusion of oxygen along the grain boundaries must be faster than through the lattice. The grain boundary diffusivity for silicon in orthopyroxenite is then given by D¯gbSiδ=(3.3±3.0)×10?9f0.0O2e?400±65/RT?m3s?1, where the activation energy for diffusion is in kJ/mol, and δ is the grain boundary width in m. Calculated growth rates for enstatite under these conditions are significantly slower than predicted by an extrapolation from similar experiments performed at 1000?°C under high pressure (hydrous) conditions by Yund and Tullis (1992), perhaps due to water-enhancement of diffusion in their experiments. 相似文献
5.
周口店地区的古环境变化研究多数研究集中在中更新世时期,而缺乏对早更新世时期环境变化的研究。这主要是由于缺少保存完好的早更新世沉积记录造成的。随着对20世纪80年代在周口地区发现的东洞剖面,发现这是一个保存完好的早更新世剖面,为研究早更新世时期的古环境变化特征提供了良好的研究材料。为了重建早更新世时期的古环境变化特征,利用XRF对东洞洞穴沉积物的主要元素（SiO2,Al2O3,Fe2O3和CaO）的化学组成进行了高分辨率分析,同时对沉积物中的FeO含量进行了测试。结果显示东洞剖面沉积物的主要化学组成为SiO2,占41.6%～58.9%,其次是Al2O3和Fe2O3,其含量的变化范围分别为13.69%～29.63%和5.00%～9.81%。Al2O3和Fe2O3在剖面上与SiO2含量成明显的镜像变化关系,显示出Al2O3和Fe2O3对沉积物中SiO2含量的稀释作用。另外,Fe2O3与Al2O3在剖面上具有很好的相关性,表明Fe2O3主要富集在富铝的矿物中。从元素含量在剖面的上分布看,东洞剖面的化学组成发生3次大的波动,主要表现为SiO2和FeO含量增高,而Fe2O3与Al2O3含量的减少。这3次波动分别出现在剖面的15.3～14.6m,11.0～9.9m和8.40～7.84m深度处。在3次化学组成的波动出现的同时,指示沉积物风化程度和温度变化的Si/Al（SiO2/Al2O3）和FeO/Fe2O3比值也发生了明显变化,比值增高,指示了3次大的干冷事件。另外,在剖面上部（10.00～7.84m,即第2次事件以后）SiO2/Al2O3和FeO/Fe2O3比值变高且波动频繁,表明自第2次干冷事件后沉积区的环境变得不稳定,逐渐向冷干气候转变。东洞剖面的地球化学记录（SiO2/Al2O3和FeO/Fe2O3）与泾川黄土剖面的粒度曲线具有较好的对比性,支持了东洞剖面记录的环境信息与黄土沉积记录的环境变化具有一致性。通过与泾川粒度曲线的对比发现,东洞剖面记录的3次干冷事件在时段上分别对应于黄土-古土壤序列中的L26,L15和L13。 相似文献
6.
Geochemical and mineralogical investigations have been carried out on laterite profiles developed in the Lake Sonfon Au district of northern Sierra Leone. The area is underlain by Archean metavolcanics and constitutes part of the Sula Mountains greenstone belt, which is mineralized in Au. Extensive lateritization has affected the rocks of this region, resulting in a profile which from bottom to top consists typically of a decomposed bedrock zone, a pisolitic laterite layer and a duricrust layer. Both the pisolitic and duricrust layers of the laterite are sometimes punctuated by lenses of ironstones containing high amounts of Cu, Zn, Ni, Co and Ce. Gold occurs as small grains within the heavy mineral fraction recovered from the decomposed rock zones and pisolitic layers of the profiles and also in gravels of streams draining the area. The mineralogy of the duricrust and pisolitic layers is dominated by goethite, gibbsite and quartz, with minor amounts (<5% by volume) of ilmenite, magnetite, haematite, rutile and kaolinite. The kaolinite content increases towards the decomposed rock zone, where talc, vermiculite and other layer lattice silicates become abundant. The heavy-mineral fraction of stream sediments is composed essentially of ilmenite, magnetite, haematite, and traces of rutile, zircon, tourmaline and Au. The Au grains are often characterized by a 10–200-μm-wide rim having a much lower content of Ag (0.3 wt.% or lower) than the grain interior (about 5 wt.% on average). Dissolution effects are also observed on the grain surfaces. It is considered that Au derived from the amphibolite parent rock is dissolved, transported, and redeposited during laterization.The duricrust cover of the laterite profiles is characterized by high contents of Fe2O3 (ca. 60 wt.%) and Al2O3 (ca. 32wt.%) and low content of SiO2 (ca. 9 wt.%). In comparison, the pisolitic layer is higher in SiO2 (ca. 18 wt.%) as well as a slightly higher in Al2O3 (ca. 34 wt.%). Lateritic weathering has resulted in the removal of CaO, Na2O, MgO and SiO2, with relative enrichment of Fe2O3 and Al2O3. The geochemical distribution of the trace elements in the laterite profiles can be related to the occurrence of the auriferous mineralization. The significance of these observations is discussed in relation to the origin of the lateritic Au and the role of the associated trace elements as indicators of the mineralization. 相似文献
7.
Kinetics of diffusion-controlled growth of fayalite 总被引：1，自引：0，他引：1
The rate of growth of fayalite (Fe2SiO4) has been measured at one atmosphere total pressure, temperatures from 1000° to 1120° C, and oxygen fugacities controlled by CO/CO2 gas-mixing from 10-9.9 to 10-13.0atm, chosen to span the fayalite stability field. The fine-grained polycrystalline fayalite layer was formed by reacting the oxides FeO or Fe3O4 with a thin slice of single-crystal quartz. The rate of growth of the fayalite increases with increasing temperature and decreasing oxygen fugacity, and is consistent with a parabolic rate law, indicating that the growth rate is controlled by diffusion through the fayalite. Microstructural observations and platinum marker experiments suggest that the reaction phase is formed at the quartz-fayalite interface, and is therefore controlled by the diffusion of iron and oxygen. The parabolic rate constant was analyzed in terms of the oxide activity gradient to yield mean chemical diffusivities for the rate-limiting ionic species, assuming bulk transport through the fayalite layer. Given that iron diffusion in olivine polycrystals occurs either by lattice diffusion, which shows a positive dependence on oxygen activity, or by grain boundary diffusion, which would result in growth rates significantly faster than we observe, we conclude that the diffusivities derived in this study represent oxygen diffusion. However, since oxygen lattice diffusion in fayalite has been established to be much slower than our measurements, it is likely that the transport path for oxygen is along the grain boundaries. Thus, the mean grain boundary diffusivity of oxygen in fayalite $\bar D$ O gb (m2 s-1), using the measured grain size of 0.25 μm, is then given by $$\bar D_O^{gb} {\mathbf{ }}\delta = 1.28 \times 10^{ - 3} f_{O_2 }^{ - 0.17} {\mathbf{ }}e^{ - 540/RT} $$ , where δ is the grain boundary width (in m), and the activation energy is in kJ/mol. Assuming δ=10-9 m (Ricoult and Kohlstedt 1983), the oxygen grain boundary diffusivities are about a factor of 30 × slower than those reported by Watson (1986) for Fo90 olivine. 相似文献
8.
Geochemical Fingerprint and Iron Ore Potential of the Siliceous Itabirite from Palaeoproterozoic Nyong Series,Zambi Area,Southwestern Cameroon 
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下载免费PDF全文 Sylvestre Ganno Cyriel Moudioh Adjija Nzina Nchare Gus Djibril Kouankap Nono Jean Paul Nzenti 《Resource Geology》2016,66(1):71-80
The study area forms part of an emerging iron ore province of southern Cameroon. Geochemistry analyses reveal that the siliceous itabirite has a very simple chemical composition, with Fe2O3 and SiO2 representing more than 96 wt.% of the average composition; suggesting chemical precipitates of silica and iron. Low Al2O3 and TiO2 concentrations and a weak positive correlation between them point to a minor detrital component in the precipitated marine sediments. The Si/Al ratio (average 52.7) indicates the hydrothermal origin of the studied itabirite. The Al–Si discrimination diagram supports this interpretation through the plot of all data in the hydrothermal field. The studied samples have low iron content (about 39.32% Fe), high gangue content (40.97% SiO2 and 1.3 % Al2O3) and low concentration of the deleterious elements (0.16 % P and < 0.01% S). The main gangue mineral is silica which can be efficiently removed from iron ores during preparation of raw materials for the blast furnace process. According to commercial standards for crude iron ores, it may be concluded that the Zambi iron ores are a low‐grade magnetic ore that can be profitably exploited for the production of iron for steel production. 相似文献
9.
Ray Macdonald Bogus?aw Bagiński Fiorenzo Ronga Piotr Dzier?anowski Michele Lustrino Andrea Marzoli Leone Melluso 《Mineralogy and Petrology》2012,104(3-4):163-175
Matrix glass and melt inclusions in phenocrysts from pantellerite lavas of the Boseti volcanic complex, Ethiopia, record extreme fractionation of peralkaline silicic magma, with Al2O3 contents as low as 2.3?wt.%, FeO* contents up to 17?wt.% and SiO2 contents ~65?wt.%. The new data, and published data for natural and experimental glasses, suggest that the effective minimum composition for peralkaline silicic magmas has ~5?wt.% Al2O3, 13?wt.% FeO* and 66?±?2?wt.% SiO2. The dominant fractionating assemblage is alkali feldspar?+?fayalite?+?hedenbergite?+?oxides?±?quartz. Feldspar – melt relationships indicate that the feldspar is close to the minimum on the albite-orthoclase solid solution loop through the entire crystallization history. There is petrographic, mineralogical and geochemical evidence that magma mixing may have been a common process in the Boseti rhyolites. 相似文献
10.
Fang Huang Justin Glessner Adam Ianno Craig Lundstrom Zhaofeng Zhang 《Chemical Geology》2009,268(1-2):15-23
To provide inter-lab comparison for high-precision Mg isotope analysis, Mg isotope compositions (expressed as δ26Mg relative to DSM-3) for commercially accessible peridotite, basalt, andesite, and granite geo-standards have been measured by multi-collector inductively coupled mass-spectrometry (Nu-Plasma) using sample-standard bracketing method. There is a large tolerance of matrix cations during the measurement of Mg isotopes, as intensity ratios of 23Na/24Mg and 27Al/24Mg of about 20% only change the δ26Mg by less than 0.1‰, and low 55Mn/24Mg (<0.1) and 58Ni/24Mg (<0.01) do not cause significant mass bias either. Concentration match between samples and standards within 90% is adequate to obtain accurate isotope analysis, which also mitigates the isobaric interference of 12C14N+ on 26Mg. Organic matrix from chemical purification can cause significant analytical errors when the mass of Mg processed is small. The long-term reproducibility of δ26MgDSM-3 for samples with relatively higher MgO content is about 0.11‰ (2SD), and granites with lower MgO content is about 0.2‰ (2SD). Although the standards in this study have wide ranges of major element compositions with SiO2 from 40 to 70 wt.% and MgO from 0.75 to 49.6 wt.%, they exhibit a variation of Mg isotopic compositions with δ26Mg from −0.07 to −0.40‰. δ26Mg do not correlate with SiO2 or MgO contents, suggesting homogenous Mg isotope compositions in igneous rocks at the level of current precision, relative to low temperature samples including sediments and riverine and sea waters. Our data do not support a non-chondritic Mg isotope composition of the Earth. 相似文献
11.
Orange, ochre-coloured, light green and dark blue varieties of kyanite, ideally Al2SiO5, from Loliondo, Tanzania, have been characterised by electron microprobe analysis and polarised infrared and optical absorption spectroscopy. All colour varieties show elevated Fe contents of 0.39 to 1.31 wt.% FeO, but Ti contents only in the range of the EMP detection limit. Orange and ochre-coloured crystals have Mn contents of 0.23 and 0.06 wt.% MnO, respectively, the dark blue kyanite contains 0.28 wt.% Cr2O3, while the light green sample is nearly free from transition metal cations other than Fe. Polarised infrared spectra reveal OH defect concentrations of 3 to 17 wt.ppm H2O with structural OH defects partially replacing the OB (O2) oxygen atoms. Polarised optical absorption spectra show that the colour of all four varieties is governed by crystal field d-d transitions of trivalent cations, i.e. Fe3+ (all samples), Mn3+ (orange and ochre) and Cr3+ (blue kyanite), replacing Al in sixfold coordinated triclinic sites of the kyanite structure. Intervalence charge transfer, the prevalent colour-inducing mechanism in ‘usual’ (Cr-poor) blue kyanites, seems to play a very minor, if any, role in the present samples. Crystal field calculations in both a ‘classic’ tetragonal and in the semiempirical Superposition Model approach, accompanied by distance- and angle-least-squares refinements, indicate that Fe3+ preferably occupies the Al4 site, Cr3+ prefers the Al1 and Al2 sites, and Mn3+ predominantly enters the Al1 site. In each case specific local relaxation effects were observed according to the crystal chemical preferences of these transition metal cations. Furthermore, the high values obtained in the calculations for the interelectronic repulsion parameter Racah B correspond to a high ionic contribution to Me3+–O bonding in the kyanite structure. In the particular case of the blue sample, band positions specifically related to the high Racah B value enable this ‘unusual’ type of blue colouration of kyanite solely due to Cr3+ cations. 相似文献
12.
S.P.Singh K.S.V.Subramanyam C.Manikyamba M.Santosh M.Rajanikanta Singh B.Chandan Kumar 《地学前缘(英文版)》2018,9(3):769-788
The Neoarchean Bundelkhand greenstone sequences at Mauranipur and Babina areas within the Bundelkhand Gneissic Complex preserve a variety of magmatic rocks such as komatiitic basalts, basalts,felsic volcanic rocks and high-Mg andesites belonging to the Baragaon, Raspahari and Koti Formations.The intrusive and extrusive komatiitic basalts are characterized by low SiO_2(39-53 wt.%), high MgO(18-25 wt.%).moderately high Fe_2O_3(7.1-11.6 wt.%), Al_2O_3(4.5-12.0 wt.%), and TiO_2(0.4-1.23 wt.%)with super to subchondritic(Gd/Yb)N ratios indicating garnet control on the melts. The intrusive komatiitic suite of Ti-enriched and Al-depleted type possesses predominant negative Eu and positive Nb, Ti and Y anomalies. The chemical composition of basalts classifies them into three types with varying SiO_2, TiO_2, MgO, Fe_2O_3, Al_2O_3 and CaO. At similar SiO_2 content of type Ⅰ and Ⅲ basalts, the type II basalts show slightly high Al_2O_3 and Fe_2O_3 contents. Significant negative anomalies of Nb, Zr, Hf and Ti, slightly enriched LREE with relatively flat HREE and low ∑REE contents are observed in type Ⅰ and Ⅱ basalts. TypeⅢ basalts show high Zr/Nb ratios(9.8-10.4), TiO_2(1.97-2.04 wt.%), but possess strikingly flat Zr, Hf, Y and Yb and are uncontaminated. Andesites from Agar and Koti have high SiO_2(55-64 wt.%), moderate TiO_2(0.4-0.7 wt.%), slightly low Al_2O_3(7-11.9 wt.%), medium to high MgO(3-8 wt.%) and CaO contents(10-17 wt.%). Anomalously high Cr, Co and Ni contents are observed in the Koti rhyolites. Tholeiitic to calc alkaline affinity of mafic-felsic volcanic rocks and basalt-andesite dacite-rhyolite differentiation indicate a mature arc and thickened crust during the advanced stage of the evolution of Neoarchean Bundelkhand greenstone belt in a convergent tectonic setting where the melts were derived from partial melting of thick basaltic crust metamorphosed to amphibolite-eclogite facies. The trace element systematics suggest the presence of arc-back arc association with varying magnitudes of crust-mantle interaction. La/Sm, La/Ta,Nb/Th, high MgO contents(20 wt.%), CaO/Al_2O_3 and(Gd/Yb)_N 1 along with the positive Nb anomalies of the komatiite basalts reflect a mantle plume source for their origin contaminated by subductionmetasomatized mantle lithosphere. The overall geochemical signatures of the ultramafic-mafic and felsic volcanic rocks endorse the Neoarchean plume-arc accretion tectonics in the Bundelkhand greenstone belt. 相似文献
13.
《International Geology Review》2012,54(6):542-555
This paper presents new petrographic observations and geochemical and microprobe analyses for the Laomiaojishan, Xiaotongguanshan, and Tianebaodanshan intrusions in the Tongguanshan mineral district, East China. The plutons vary in composition from quartz monzonitic diorite to pyroxene monzonitic diorite, and contain gabbroic to dioritic xenoliths. The Xiaotongguanshan intrusion yields a SHRIMP zircon U–Pb age of 139.5±2.9 Ma, indicating Late Jurassic to Early Cretaceous magmatism in the Lower Yangtze River Valley. Relative to host rocks, the gabbro and diorite xenoliths are low in SiO2 (52.03–54.61 wt‐%), Al2O3 (12.87–14.43 wt‐%), and total alkalis (Na2O+K2O; 5.26–6.30 wt‐%), but high in MgO (5.41–11.66 wt‐%); the host rocks have high SiO2 (59.97–64.44 wt‐%), Al2O3 (16.43–17.59 wt‐%), and total alkalis (6.67–8.25 wt‐%), but are low in MgO (1.52–2.50 wt‐%). Concentrations of rare earth elements (REEs) in the xenoliths (165.70–190.40 ppm) are similar to those in the host rocks (166.12–185.95 ppm), although the ratio of light REEs to heavy REEs in the xenoliths (3.39–4.27) is lower than that in the host plutons (4.86–5.94). All of the analysed rocks show similar REE patterns, although the xenoliths display marked positive Eu anomalies and the host rocks show slightly negative Eu anomalies. Values of epsilon Nd (t) ranges from ?4.9 to ?9.9 in the gabbro xenoliths and from ?11.4 to ?11.9 in the host intrusives. Initial 87Sr/86Sr ratios are 0.7064–0.7073 in the xenoliths and 0.7072–0.7084 in the quartz monzonitic diorite host rocks. Crystallization temperatures of hornblende and plagioclase in the gabbro xenoliths, diorite xenoliths, and host rocks are 816, 773–790, and 664–725°C, respectively, based on an amphibole–plagioclase geothermometer. The pressures recorded by these phases indicate that they formed at depths of 26, 12–15, and 3–4 km, respectively, based on an aluminum‐in‐hornblende geobarometer. The petrological and geochemical features of the analysed intrusions and xenoliths are consistent with their derivation from basic to intermediate‐acidic magmas that possibly formed via a series of complex interactions between underplated, mantle‐derived basaltic magma and varying amounts of middle‐ to lower‐crustal material, followed by assimilation–fractional crystallization. 相似文献
14.
Vladica Cvetkovi? Suzana Eri? Ma?a Radivojevi? Kristina ?ari? 《Mineralogy and Petrology》2012,106(3-4):131-150
The study focuses on clinopyroxene from mantle xenolith-bearing East Serbian basanites and suggests that dissolution of mantle orthopyroxene played an important role in at least some stages of the crystallization of these alkaline magmas. Five compositional types of clinopyroxene are distinguished, some of them having different textural forms: megacrysts (Type-A), green/colourless-cored phenocrysts (Type-B), overgrowths and sieve-textured cores (Type-C), rims and matrix clinopyroxene (Type-D), and clinopyroxene from the reaction rims around orthopyroxene xenocrysts (Type-E). Type-A is high-Al diopside that probably crystallized at near-liquidus conditions either directly from the host basanite or from compositionally similar magmas in previous magmatic episodes. Type-B cores show high VIAl/IVAl≥1 and low Mg# of mostly <75 and are interpreted as typical xenocrysts. Type-C, D and E are interpreted as typical cognate clinopyroxene. Type-D has Mg#<78, Al2O3?=?6–13?wt.%, TiO2?=?1.5–4.5?wt.%, and Na2O?=?0.4–0.8?wt.% and compositionally similar clinopyroxene is calculated by MELTS as a phase in equilibrium with the last 30?% of melt starting from the average host lava composition. Type-C has Mg#?=?72–89, Al2O3?=?4.5–9.5?wt.%, TiO2?=?1–2.5?wt.%, Na2O?=?0.35–1?wt.% and Cr2O3?=?0.1–1.5?wt.%. This clinopyroxene has some compositional similarities to Type-E occurring exclusively around mantle orthopyroxene. Cr/Al vs Al/Ti and Cr/Al vs Na/Ti plots revealed that Type-C clinopyroxene can crystallize from a mixture of the host basanite magma and 2–20?wt.% mantle orthopyroxene. Sieve-textured Type-C crystals show characteristics of experimentally produced skeletal clinopyroxene formed by orthopyroxene dissolution suggesting that crystallization of Type-C was both texturally and compositionally controlled by orthopyroxene breakdown. According to FeO/MgOcpx/melt modelling the first clinopyroxene precipitating from the host basanite was Type-A (T?~?1250?°C, p?~?1.5?GPa). Dissolution of orthopyroxene produced decreasing FeO/MgOmelt and crystallization of Type-E and sieve-textured Type-C clinopyroxene (0.3–0.8?GPa and 1200–1050?°C). The melt composition gradually shifted towards higher FeO/MgOmelt ratios precipitating more evolved Type-C and Type-D approaching near-solidus conditions (<0.3?GPa; ~950?°C). 相似文献
15.
Suzanne Y. Wass 《Lithos》1979,12(2):115-132
Geochemical and textural data on clinopyroxenes in individual alkali basaltic flows from provinces in eastern Australia and the Massif Central can be used to differentiate four different modes of origin (three at high pressure) for these clinopyroxenes. Many single flows from the two provinces contain clinopyroxenes of three, or even four, of these origins. Rare flows contain core clinopyroxene with overgrowths of clinopyroxenes of two distinct generation. Each of the overgrowth is compositionally analogous to clinopyroxenes occurring in xenoliths or as discrete crystals in the same host lava. Such rimming relationships provide evidence that the host magma has undergone high pressure crystallisation and confirm that some xenoliths and megacrysts are cognate. With decreasing pressure the major changes in clinopyroxene chemistry are an increase in the ratio Allv/Alvi, a linear increase of atomic proportions of Ti and Al with decreasing Si, and an increase in the Ti: (100 Mg/(Mg + Σ Fe)) ratio of the pyroxenes. Al2O2 wt, % is an unreliable potential geobarometric indicator; consideration of tetrahedral and octahedral site occupancies by Al (Allv/Alvl ratio) is necessary. High-pressure fractionation dominated by clinopyroxene is postulated for some basaltic-composition, resulting in SiO2 depletion, alkali enrichment and decrease in the Mg/(Mg + Fe2+) value of the host magma. 相似文献
16.
暴露测年样品中26Al和10Be分离及其加速器质谱测定 总被引：4，自引：4，他引：0
在已有实验流程基础上,建立并优化了石英样品中Be和Al提取、纯化等实验流程,设计的流程条件实验包括实验试剂、器皿和离子交换柱选择、离子交换树脂分离Be和Al时酸浓度选择等。结果表明,选择钢铁研究总院研制的9Be标准溶液作为10Be样品制备的载体;使用一次性实验器皿;选用4 cm规格的离子交换柱;用0.05 mol/L草酸和0.75 mol/L盐酸混合溶液洗脱吸附于阴离子树脂上的Al,可有效提取、纯化样品中的Be和Al。加速器质谱(AMS)测量结果显示,13组化学空白的10Be/9Be和26Al/27Al比值平均值分别为7.48×10-15和1.96×10-15,与国内已有宇宙成因核素实验室的结果(5×10-15~8×10-15)具有可比性。电感耦合等离子体发射光谱(ICP-AES)的测量结果表明,Be、Al回收率分别达90%和60%。基于新建立的实验流程分析了祁连山北侧金佛寺的一个岩石样品,获得了10Be和26Al的暴露年代分别为(10.7±1.0) ka和(10.0±1.2) ka,与前人研究结果一致。 相似文献
17.
Mohammad Ali Rajabzadeh Teimoor Nazari Dehkordi 《Arabian Journal of Geosciences》2013,6(11):4445-4461
Neyriz ophiolite in Abadeh Tashk area appears as four major separated massifs in an area with 125 km2, south of Iran. Peridotites including harzburgite, dunite, and lesser low-Cpx lherzolite are the major constituents of the ophiolite with very minor mafic rocks. Usual gabbros of ophiolite complexes are virtually absent from the study area. Mineral modality associated with bulk rock and mineral chemistry of the peridotites show a progression from fertile to ultra-refractory character, reflected by a progressive decrease in modal pyroxenes and in Al2O3, CaO, SiO2, Sc, Ta, V, and Ga values of the studied rocks by approaching chromite deposits. The Neyriz peridotites vary from low-Cpx lherzolite (MgO, 41.97–43.1 wt.%; Al2O3, 0.8–1.3 wt.%) with low content of Cr# spinel (36.7–37.6) and Fo olivine (90.79–91.5) to harzburgite (MgO, 44.31–45.25 wt.%;Al2O3, 0.29–0.45 wt.%; Cr# spinel, 58.2–73.45; Fo olivine, 91.23–91.56), and then to dunite (MgO, 45.9–49.2 wt.%; Al2O3, 0.18–0.48 wt.%) with higher content of Cr# spinel (74.34–79.36) and Fo olivine (91.75–94.68). Compared to modern oceanic settings, mineral and rock composition of low-Cpx lherzolite plot within the field of mid-ocean-ridge environment, whereas those of harzburgite and dunite fall in the field of fore-arc peridotites. As a result of the studies on minerals and whole rock chemistry along with rock interrelationships, we contend that the peridotites were subsequently affected by percolating hydrous boninitic melt from which the high-Cr–Mg, low-Ti chromitites were formed within mantle wedge above the supra-subduction zone in a fore-arc setting. 相似文献
18.
Wenjun Yong E. Dachs A. C. Withers E. J. Essene 《Physics and Chemistry of Minerals》2006,33(3):167-177
The low-temperature heat capacity (C
p
) of KAlSi3O8 with a hollandite structure was measured over the range of 5–303 K with a physical properties measurement system. The standard entropy of KAlSi3O8 hollandite is 166.2±0.2 J mol−1 K−1, including an 18.7 J mol−1 K−1 contribution from the configurational entropy due to disorder of Al and Si in the octahedral sites. The entropy of K2Si4O9 with a wadeite structure (Si-wadeite) was also estimated to facilitate calculation of phase equilibria in the system K2O–Al2O3–SiO2. The calculated phase equilibria obtained using Perple_x are in general agreement with experimental studies. Calculated phase relations in the system K2O–Al2O3–SiO2 confirm a substantial stability field for kyanite–stishovite/coesite–Si-wadeite intervening between KAlSi3O8 hollandite and sanidine. The upper stability of kyanite is bounded by the reaction kyanite (Al2SiO5) = corundum (Al2O3) + stishovite (SiO2), which is located at 13–14 GPa for 1,100–1,400 K. The entropy and enthalpy of formation for K-cymrite (KAlSi3O8·H2O) were modified to better fit global best-fit compilations of thermodynamic data and experimental studies. Thermodynamic calculations were undertaken on the reaction of K-cymrite to KAlSi3O8 hollandite + H2O, which is located at 8.3–10.0 GPa for the temperature range 800–1,600 K, well inside the stability field of stishovite. The reaction of muscovite to KAlSi3O8 hollandite + corundum + H2O is placed at 10.0–10.6 GPa for the temperature range 900–1,500 K, in reasonable agreement with some but not all experiments on this reaction. 相似文献
19.
D. Berggren Kleja W. Standring D.H. Oughton K. Fifield 《Geochimica et cosmochimica acta》2005,69(22):5263-5277
The solubility of aluminium (Al) in many acidic soils is controlled by complexation reactions with soil organic matter. In such soils, Al solubility is theoretically a function of the pool size of “active” Al, i.e., the total amount of Al that equilibrates with the soil solution within a defined period of time. To date, no reliable measurements of “active” Al in soil materials exist. In this study, we determined the isotopically exchangeable pool of Al (EAl) as an operationally defined assessment of “active” Al in acidic mineral soils. The suitability of CuCl2 and pyrophosphate (Na4P2O7) as extractants for “active” Al was also evaluated. Eleven samples, mostly from spodic B horizons, were spiked with carrier-free 26Al and equilibrated for different time periods (1-756 h). The size of the Al pool with which the 26Al tracer exchanged increased with time during the whole experimental period. Thus, contact time between solid and solution phases needs to be defined when assessing the “active” Al pool. Values of EAl obtained after 1 to 5 d of equilibration were equal to the amount of CuCl2 extractable Al, but considerably smaller than the Na4P2O7-extractable pool. Equilibration times greater than 5 d resulted in CuCl2 extractable Al concentrations that under-estimated the “active” Al pool. Three of the investigated samples were rich in imogolite-type materials (ITM). In these samples, 30-50 % of the added 26Al rapidly became associated with soil constituents in forms that could not be extracted by Na4P2O7, indicating that a part of ITM may be in a dynamic state. 相似文献
20.
Porcelain wares have been produced following the directions contained in the Heylyn and Frye patent of 1744, using Cherokee clay and a lime‐alkali glass frit. The wares were fired to the bisque (˜ 950°C), glazed using a clay‐glass mixture, and then fired to a “heat‐work” level of Orton cone 9–90° deflection at 150°C per hour (1279°C). Modal mineralogy comprises Caplagioclase and two glass phases, one relict frit and the other a melt phase. The bulk chemistry of the body comprises 64.3 wt % SiO2, 21.7 wt % Al2O3, and 5.6 wt % CaO. Molecular ratios are SiO2:Al2O3 5.0 and SiO2:CaO 10.7. It is concluded that the patent, whose significance has been questioned over many years, was a practical working recipe, that close comparison may be made with porcelains of the “A”‐marked group, and that the patent represents a remarkable landmark in English ceramic history. © 2004 Wiley Periodicals, Inc. 相似文献