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1.
核废物地质处置中热-水-应力耦合对迁移影响的三维有限元模拟 总被引：1，自引：0，他引：1
将所建立的热-水-应力-迁移耦合模型及开发的有限元程序,由二维分析拓展到三维分析,并从方法论研究的角度,以一个简单的核废物地质处置模型为算例,进行热-水-应力-迁移耦合过程的三维数值模拟,考察了近场的温度、饱和度、核素浓度、孔隙水压力、位移、正应力、流速等的分布与变化,认为计算结果符合规律,得出了若干结论：为了精确地模拟放射性核素迁移,就必须将温度场、渗流场、应力场和核素浓度场进行耦合分析;核废物埋存若干年后将在处置孔壁附近产生较高的压应力;缓冲层内各点的核素浓度达到相对稳定的时间要比温度和饱和度达到相对稳定的时间长得多。 相似文献
2.
铀在北山花岗岩中的吸附迁移影响因素研究 总被引：1，自引：0，他引：1
运用水文地球化学模拟软件PHREEQC-Ⅱ,对铀元素进入中国高放废物处置预选场研究区地下水后的状况进行了模拟和预测。模拟得到核素铀进入研究区地下水后的元素浓度分布和迁移情况及外界因素变化引起地下水中铀迁移的行为,同时采用批式法测定不同条件下铀在甘肃北山花岗岩中的分配系数,研究了岩石粒径、溶液初始浓度、水相pH和温度对分配系数的影响,实验结果表明花岗岩对铀的吸附能力较弱,其中溶液初始浓度、粒径、温度影响较小,pH值对岩石的吸附性能有较大影响,在接近中性条件下影响达到最大,这与采用模拟软件模拟结果基本吻合。通过模拟和实验对比,能更好地研究在北山预选区处置条件下地下水-废物-岩石的相互作用过程中核素的迁移行为,从而为处置库系统安全评价提供有关依据。 相似文献
3.
非平衡吸附放射性核素迁移数值模型研究 总被引：3，自引：0，他引：3
放射性核素在以水作为载体于多孔介质中迁移时，吸附与解吸作用不容忽视．吸附与解吸为一非平衡过程，本文建立了考虑非平衡吸附的放射性核素迁移数植模型，模型中对于水动力弥散方程和非平衡吸附关系式的耦合，采用数值离散、直接代入的方法使数值求解便于实施．利用现场核素迁移试验观测资料对所建立的非平衡吸附核素迁移数值模型进行了检验，充分说明了该模型的有效性． 相似文献
4.
高放废物地质处置过程中涉及的核素在围岩裂隙地下水中的迁移问题已引起广泛关注,数值模拟是研究核素粒子运移的重要方法。目前裂隙介质中渗流模型主要是等效连续介质模型、双重介质模型和离散裂隙网络模型。对于岩体尺度裂隙地下水的流动,离散裂隙网络模型能充分表现裂隙介质的各向异性、不连续性等特征。因此,针对裂隙介质准确概化及核素迁移模拟等难点,文章结合Monte Carlo随机生成裂隙方法、裂隙渗流有限元算法和高放射性核素衰变方程等方法,依据花岗岩深钻孔裂隙统计数据,采用离散裂隙网络模型对内蒙古阿拉善高放废物地质处置预选区展开了核素粒子迁移数值模拟研究,并讨论了实例预测分析结果。结果显示:针对设定的地质模型,核素粒子从中心运移到边界的迁移路径长度平均为1293.35 m,粒子运移到边界耗费的时间平均为1.70E+11 d。 相似文献
5.
热-水-应力耦合条件下三项因素对核素迁移影响的有限元分析 总被引：3，自引：2，他引：1
目前在放射性核素随地下水迁移的研究中还很少涉及温度场和应力场的影响。针对这一问题,引入渗透迁移方程,将所开发的饱和-非饱和孔隙介质中热-水-应力耦合弹塑性模型及其二维有限元程序进行了扩展和改进,使之可以同步地对温度场、渗流场、应力场和放射性核素浓度场的变化进行解析。对一个假想的核废料处置库算例,通过分别改变影响地下水中核素迁移的3个因素：渗透系数、分配系数和分子扩散系数,考察了在热-水-应力-迁移耦合作用条件下近场放射性核素浓度的分布及变化,从而认识到：当缓冲层的渗透系数小到一定程度后,缓冲层中核素迁移基本不再受渗流场的影响;缓冲层分配系数越小,分子扩散系数越大,核素迁移越快。 相似文献
6.
随着世界各国大力发展核电，放射性废料的安全处置已成为当今研究热点和前沿学科。高放废物深地质处置的安全性主要取决于处置库内放射性核素向生物圈的迁移程度。在侵入岩中，放射性核素主要是通过地下水沿岩石孔隙从处置库向生物圈迁移的。为了理解放射性核素在花岗岩体接触带的迁移行为，本文根据两花岗岩体接触带中样品的铀系核素放射性活度比值（^234U/^238U,^230Th/^234U,^226Ra/^230Th,^230Th/^238U)，利用 α-反冲（弹射）作用引起的放射性不平衡理论，计算了铀系核素子体^234U,^230Th,^226Ra在后期地下水的作用下在花岗岩体接触带及其裂隙内的迁出率、迁入率、并进行了质量平衡的计算。结果表明，经α-反冲作用进入流体的核素的迁出率要远大于因核素自然衰变的消亡率；裂隙充填物及裂隙能阻滞大量核素的迁移，其沉淀核素来自接触带花岗岩；花岗岩能强烈阻滞核素的迁移，可作为阻止放射性核素从核废料地下处置库向外迁移的有利天然屏障。 相似文献
7.
将铀尾矿库核素迁移问题概括为均质多孔介质中稳定的二维水流条件下的三维溶质迁移问题,利用Visual Modflow软件（MT3D）采用全隐式差分法对某铀尾矿库放射性核素迁移进行了模拟研究,模拟值结果与浓度实测值较吻合,揭示了尾矿库放射性核素时空迁移规律。 相似文献
8.
9.
核素在裂隙介质中的迁移问题是核废物深地质处置中极为关注的问题。为了解裂隙介质中核素的迁移规律,建立了基于双重介质理论的描述核素在裂隙域和基质域中迁移的基本微分方程,利用拉普拉斯变换推导出其解析解;在对西北某核废物处置场预选区地水文地质条件分析的基础上,获取相关参数,利用一维多途径核素迁移模型,选取国内在花岗岩中研究较多的核素Cs-134、Co-57、Tc-99,模拟这几种核素的相对浓度随模拟时间、迁移距离的变化规律。模拟结果表明：在其他条件都相同的情况下,Cs-134的迁移是最快的,而Tc-99迁移是最慢的。 相似文献
10.
基岩裂隙水中90Sr迁移的数值模拟 总被引：2，自引：0，他引：2
针对我国西北某放射性废物处置场的水文地质情况,通过渗透张量系数计算和溶质迁移参数测试,建立了基岩裂隙水渗透模型和90Sr在基岩裂隙水中的迁移模型.根据以上两个模型的耦合,采用有限差分法,利用MODFLOW软件对90Sr进入处置场地下水后的迁移情况进行了数值模拟预测.计算结果表明,由于机械弥散、对流作用、地质介质的吸附阻滞作用以及核素本身的衰变作用,处置库运行100a后因破坏而导致核素90Sr进入地下水后的有害污染面积比较小,不会对水井及下游造成不利的影响. 相似文献
11.
Calculated Phase Relations in the System NCKFMASH (Na2O-CaO-K2O-FeO-MgO-Al2O3-SiO2-H2O) for High-Pressure Metapelites 总被引：5，自引：0，他引：5
Petrogenetic grids in the system NCKFMASH (Na2O–CaO–K2O–FeO–MgO–Al2O3–SiO2–H2O)and the subsystems NCKMASH and NCKFASH calculated with the softwareTHERMOCALC 3.1 are presented for the P–T range 7–30kbar and 450–680°C, for assemblages involving garnet,chloritoid, biotite, carpholite, talc, chlorite, kyanite, staurolite,paragonite, glaucophane, jadeite, omphacite, diopsidic pyroxene,plagioclase, zoisite and lawsonite, with phengite, quartz/coesiteand H2O in excess. These grids, together with calculated compatibilitydiagrams and P–T and T–XCa and P–XCa pseudosectionsfor different bulk-rock compositions, show that incorporationof Ca into the NKFMASH system leads to many of the NKFMASH invariantequilibria moving to lower pressure and/or lower temperature,which results, in most cases, in the stability of jadeite andgarnet being enlarged, but in the reduction of stability ofglaucophane, plagioclase and AFM phases. The effect of Ca onthe stability of paragonite is dependent on mineral assemblageat different P–T conditions. The calculated NCKFMASH diagramsare powerful in delineating the phase equilibria and P–Tconditions of natural pelitic assemblages. Moreover, contoursof the calculated phengite Si isopleths in P–T and P–XCapseudosections confirm that phengite barometry in NCKFMASH isstrongly dependent on mineral assemblage. KEY WORDS: phase relations; metapelites; NCKFMASH; THERMOCALC; phengite geobarometry 相似文献
12.
Smriti SinghLal C. Ram Reginald E. MastoSantosh K. Verma 《International Journal of Coal Geology》2011,87(2):112-120
Coal being a limited source of energy, extraction of energy from other sources like lignite, coal-refuse, and biomass is being attempted worldwide. The minerals and inorganic elements present in fuel feeds pose different technological and environmental concerns. Lignite ash, refuse ash, and biomass ash collected from Indian power plants burning lignite, coal-refuse, and mustard stalk, respectively, were analyzed for physico-chemical characteristics and trace elements. The lignite ash has high SiO2, CaO, MgO, Al2O3, and SO3; the refuse ash has high SiO2 and Fe2O3, but low SO3; the biomass ash has high SiO2 (but low Al2O3), and high CaO, MgO, K2O, Na2O, SO3, and P2O5. A substantial presence of chloride (2.1%) was observed in the biomass ash. Quartz is the most abundant mineral species. Other minerals are mullite, hematite, gehlenite, anhydrite, and calcite in the lignite ash; orthoclase in the refuse ash; albite, sanidine, gehlenite, anhydrite, and calcite in the biomass ash. Ashes with high concentrations (> 100 mg/kg) of trace elements are: lignite ash (V < La < Mn < Cr < Ni < Nd < Ba < Ce, Zn < Sr); refuse ash (Cr < Ce < V < Rb < Mn < Sr, Zn < Ba); biomass ash (Cu < Zn < Ba, Sr). Based on Earth crust normalization, Co, Ni, As, Se, Mo, Zn, Pb, U, and REEs (except Pr and Er) are enriched in the lignite ash; molybdenum, Zn, Cs, Pb, Th, U, La, Ce, and Lu in the refuse ash; and Mo, Zn, Sr, Cs, Pb, and Lu in the biomass ash. Elements As, Zn, Mo, Ni, Pb, Rb, Cr, V, Ba, Sr, and REEs are correlated with Al, indicating the possibilities of their association with aluminum silicates minerals. Similarly, barium, Cs, Th, and U are correlated with iron oxides; molybdenum and Sr may also be associated with sulfates and chlorides. Due to the alkaline nature of these ashes, the high concentrations of As and Se in the lignite ash; molybdenum in the biomass ash; and Se in the refuse ash may pose environmental concerns. 相似文献
13.
The Cu–Co–Ni Texeo mine has been the most important source of Cu in NW Spain since Roman times and now, approximately 40,000 m3 of wastes from mine and metallurgical operations, containing average concentrations of 9,263 mg kg−1 Cu, 1,100 mg kg−1 As, 549 mg kg−1 Co, and 840 mg kg−1 Ni, remain on-site. Since the cessation of the activity, the abandoned works, facilities and waste piles have been posing
a threat to the environment, derived from the release of toxic elements. In order to assess the potential environmental pollution
caused by the mining operations, a sequential sampling strategy was undertaken in wastes, soil, surface and groundwater, and
sediments. First, screening field tools were used to identify hotspots, before defining formal sampling strategies; so, in
the areas where anomalies were detected in a first sampling stage, a second detailed sampling campaign was undertaken. Metal
concentrations in the soils are highly above the local background, reaching up to 9,921 mg kg−1 Cu, 1,373 mg kg−1 As, 685 mg kg−1 Co, and 1,040 mg kg−1 Ni, among others. Copper concentrations downstream of the mine works reach values up to 1,869 μg l−1 and 240 mg kg−1 in surface water and stream sediments, respectively. Computer-based risk assessment for the site gives a carcinogenic risk
associated with the presence of As in surface waters and soils, and a health risk for long exposures; so, trigger levels of
these elements are high enough to warrant further investigation. 相似文献
14.
The Cretaceous deposits of the Southern Petén Basin, an oil-producing province, are located to the south of the Yucatan Platform and to the east of the Chiapas Carbonate Platform of Mexico. The succession in the southern part of this basin has been studied both in wells and at outcrop by microfacies analysis. It is composed of 5000 m of shallow marine carbonates and evaporites with a few thin layers of pelagic limestones rich in organic carbon and planktic foraminifera deposited during peak transgressions or maximum flooding. The sedimentation of this thick succession was not continuous, and the section is punctuated by subaerial erosional bounding surfaces and a single hardground which marks the final drowning of the carbonate platform during the late Maastrichtian. New age determinations have been obtained on the basis of planktic and benthic foraminifera from the Aptian to Santonian Cobán Formation, D, C, B and A Members. Cobán C (Albian) and B (Cenomanian) Members are the present oil reservoirs. The rudist and alveolinid limestones of late Campanian and Maastrichtian age referred to the Campur Formation in the Southern Petén Basin are here reassigned to the Angostura Formation, as recognized in the Chiapas area. The Actela Formation is defined here to encompass the limestone breccia deposits that occur at the Cretaceous–Tertiary boundary and extend into the Parvularugoglobigerina eugubina Zone of early Danian age. The D, C, B and A Members of the Cobán Formation and the Angostura Formation represent second order transgressive and regressive trends in a passive margin area where the deposits indicate a succession of various environments, including fluviatile, salinas, shallow marine carbonate platform, outer shelf and intrashelf basin. High subsidence rates, sea-level changes and tectonic uplift controlled the sedimentation.
Abstract
Les formations crétacées du sud-est du Bassin du Petén, région pétrolière du nord du Guatemala, sont situées au Sud du Yucatan et à l'Est du Chiapas au Mexique. Ces sédiments ont été étudiés à la fois dans deux puits et à l'affleurement par l'analyse des microfaciès. Cet ensemble sédimentaire est composé de 5000 m de carbonates de plate-forme de faible profondeur et d'évaporites, dans lesquels s'intercalent de minces couches de calcaires pélagiques riches en matière organique et en foraminifères planctoniques. Ces calcaires pélagiques se sont déposés lors des maximums de transgressions. La sédimentation de cette épaisse série n'est pas continue et est ponctuée par quelques surfaces d'érosion sub-aérienne et une surface durcie qui souligne l'ennoyage définitif de la plate-forme carbonatée au Maastrichtien terminal. De nouvelles datations ont été obtenues sur la formation Cobán et ses membres D, C, B et A qui s'étagent de l'Aptien au Santonien. Les membres C (albien) et B (cénomanien) constituent les réservoirs productifs. Les calcaires à rudistes et à alveolinidés du Campanien supérieur–Maastrichtien ont été appelés à tort au Petén formation Campur. Ils doivent, selon nous, être attribués à la formation Angostura comme au Chiapas voisin, où affleurent des faciès comparables et de même âge. Une nouvelle formation est créée (formation Actela) pour les brèches calcaires de la limite Crétacé–Tertiaire et de la Zone à Eugubina du Danien inférieur. Les membres D, C, B, A de la formation Cobán et la formation Angostura représentent des cycles transgressifs–régressifs de deuxième ordre. Sur cette marge passive du Petén, les dépôts correspondent à des environnements variés comme des terres émergées soumises à une altération karstique et à des dépôts fluviatiles, des salinas, des plates-formes carbonatées marines, des shelf externes et des bassins intra plate-forme. La sédimentation a été, ici, contrôlée par une forte vitesse de subsidence, les variations du niveau marin et des soulèvements tectoniques. 相似文献15.
Structural parameters and cation ordering are determined for four compositions in the synthetic MgGa2O4-Mg2GeO4 spinel solid solution (0, 8, 15 and 23 mol% Mg2GeO4; 1400 °C, 1 bar) and for spinelloid β-Mg3Ga2GeO8 (1350 °C, 1 bar), by Rietveld refinement of room-temperature neutron diffraction data. Sample chemistry is determined by
XRF and EPMA. Addition of Mg2GeO4 causes the cation distribution of the MgGa2O4 component to change from a disordered inverse distribution in end member MgGa2O4, [4]Ga = x = 0.88(3), through the random distribution, toward a normal cation distribution, x = 0.37(3), at 23 mol% Mg2GeO4. An increase in ao with increasing Mg2GeO4 component is correlated with an increase in the amount of Mg on the tetrahedral site, through substitution of 2 Ga3+⇄ Mg2++Ge4+. The spinel exhibits high configurational entropy, reaching 20.2 J mol−1 (four oxygen basis) near the compositional upper limit of the solid solution. This stabilizes the spinel in spite of positive
enthalpy of disordering over the solid solution, where ΔH
D
= αx + βx
2, α = 22(3), β = −21(3) kJ mol−1. This model for the cation distribution across the join suggests that the empirically determined limit of the spinel solid
solution is correlated with the limit of tetrahedral ordering of Mg, after which local charge-balanced substitution is no
longer maintained.
Spinelloid β-Mg3Ga2GeO8 has cation distribution M1[Mg0.50(2)Ga0.50(2)] M2[Mg0.96(2)Ga0.04(2)] M3[Mg0.77(2) Ga0.23(2)]2 (Ge0.5Ga0.5)2O8 (tetrahedral site occupancies are assumed). Octahedral site size is correlated to Mg distribution, where site volume, site
distortion, and Mg content follow the relation M1<M3<M2. The disordered cation distribution provides local electrical neutrality
in the structure, and stabilization through increased configurational entropy (27.6 J mol−1; eight oxygen basis). Comparison of the crystal structures of Mg1+
N
Ga2−2
N
Ge
N
O4 spinel, β-Mg3Ga2GeO8, and Mg2GeO4 olivine reveals β-Mg3Ga2GeO8 to be a true structural intermediate. Phase transitions across the pseudobinary are necessary to accommodate an increasing
divergence of cation size and valence, with addition of Mg2GeO4 component. Octahedral volume increases while tetrahedral volume decreases from spinel to β-Mg3Ga2GeO8 to olivine, with addition of Mg and Ge, respectively. Furthermore, M-M distances increase regularly across the join, suggesting
that changes in topology reduce cation-cation repulsion.
Received: 9 November 1998 / Revised, accepted: 3 August 1999 相似文献
16.
Geochemistry constraints of Mesozoic–Cenozoic calc-alkaline magmatism in the South Shetland arc, Antarctica 总被引：1，自引：0，他引：1
A. Machado E.F. Lima F. Chemale Jr. D. Morata O. Oteiza D.P.M. Almeida A.M.G. Figueiredo F.M. Alexandre J.L. Urrutia 《Journal of South American Earth Sciences》2005,18(3-4):407-425
Geochemical data from basalts, basaltic andesites, and andesites of the Mesozoic–Cenozoic (143–44 Ma) from Livingston, Greenwich, Robert, King George, and Ardley Islands of the South Shetland archipelago, Antarctica, are presented. The rocks have variable SiO2 of approximately 46–61 wt%, Al2O3 of 15–26 wt%, and total alkali (K2O+Na2O) of 2–6 wt%. Most samples have low Mg#, Cr, and Ni, which indicates that they have undergone significant fractional crystallization from mantle-derived melts. The presence of olivine cumulatic in the samples from Livingston and Robert Islands explains some high MgO, Ni, and Cr values, whereas low Rb, Zr, and Nb values could be related to undifferentiated magmas. N-MORB-normalized trace element patterns show that South Shetland Islands volcanic rocks have a geochemical pattern similar to that found for other island arcs, with enrichment in LILE relative to HFSE and in LREE relative to HREE. The geochemistry pattern and presence of calcic plagioclase, orthopyroxene, Mg-olivine, and titanomagnetite phenocrysts suggest a source related to the subduction process. The geochemical data also suggest magma evolution from the tholeiitic to the calc-alkaline series; some samples show a transitional pattern. Samples from the South Shetland archipelago show moderate LREE/HREE ratios relative to N-MORB and OIB, depletion in Nb relative to Yb, and high Th/Yb ratios. These patterns probably reflect magma derived from a lithospheric mantle source previously modified by fluids and sediments from a subduction zone.
Resumo
Dados geoquímicos de basaltos, andesitos basálticos e andesitos mesozóicos–cenozóicos (143–44 Ma) das ilhas Livingston, Greenwich, Robert, King George e Ardley do Arquipélago Shetland do Sul, Antártica são discutidas neste artigo. As rochas tem conteúdos de SiO2 variando de 46 a 61%, Al2O3 de 15 a 26% e álcalis (K2O+Na2O) de 2 a 6%. A maior parte das amostras tem conteúdos baixos de Mg#, Cr e Ni, indicando que sofreram significante cristalização fracionada de fusões derivadas do manto. A presença de fases cumuláticas nas amostras das ilhas Livingston e Robert explicaria os elevados valores de MgO, Ni, Cr, enquanto que baixos valores de Rb, Zr e Nb observados nas amostras destas ilhas poderiam estar relacionados a magmas não diferenciados. Os padrões de elementos-traço normalizados pelo N-MORB mostram que as rochas vulcânicas das Ilhas Shetland do Sul têm padrão geoquímico similar àqueles encontrados em outros arcos de ilhas com enriquecimento em LILE em relação aos HFSE e em ETRL em relação aos ETRP. O padrão geoquímico e a ocorrência de fenocristais de plagioclásio cálcico, ortopiroxênio, olivina magnesiana e titanomagnetita sugerem origem relacionada a processos de subducção. Dados geoquímicos obtidos para as amostras do arquipélago Shetland do Sul sugerem um magma evoluindo de toleítico para cálcico-alcalino, observando-se em algumas amostras um padrão transicional. As amostras do arquipélago Shetland do Sul mostram em relação ao N-MORB e OIB, moderadas razões ETRL/ETRP, empobrecimento em Nb relativo a Yb e elevada razão Th/Yb Estes padrões refletem, provavelmente, magma derivado de uma fonte mantélica litosférica, que foi modificada por fluídos e sedimentos da zona de subducção. 相似文献17.
Dirk Frei Axel Liebscher Gerhard Franz Bernd Wunder Stephan Klemme Jon Blundy 《Contributions to Mineralogy and Petrology》2009,157(4):473-490
We determined experimentally the Nernst distribution coefficient between orthopyroxene and anhydrous silicate melt for trace elements i in the system Na2O–CaO–MgO–Al2O3–SiO2 (NCMAS) along the dry model lherzolite solidus from 1.1 GPa/1,230°C up to 3.2 GPa/1,535°C in a piston cylinder apparatus.
Major and trace element composition of melt and orthopyroxene were determined with a combination of electron microprobe and
ion probe analyses. We provide partitioning data for trace elements Li, Be, B, K, Sc, Ti, V, Cr, Co, Ni, Rb, Sr, Y, Zr, Nb,
Cs, Ba, La, Ce, Sm, Nd, Yb, Lu, Hf, Ta, Pb, U, and Th. The melts were chosen to be boninitic at 1.1 and 2.0 GPa, picritic
at 2.3 GPa and komatiitic at 2.7 and 3.2 GPa. Orthopyroxene is Tschermakitic with 8 mol% Mg-Tschermaks MgAl[AlSiO6] at 1.1 GPa while at higher pressure it has 18–20 mol%. The rare earth elements show a continuous, significant increase in
compatibility with decreasing ionic radius from D
Laopx−melt ∼ 0.0008 to D
Luopx−melt ∼ 0.15. For the high-field-strength elements compatibility increases from D
Thopx−melt ∼ 0.001 through D
Nbopx−melt ∼ 0.0015, D
Uopx−melt ∼ 0.002, D
Taopx−melt ∼ 0.005, D
Zropx−melt ∼ 0.02 and D
Hfopx−melt ∼ 0.04 to D
Tiopx−melt ∼ 0.14. From mathematical and graphical fits we determined best-fit values for D
0M1, D
0M2, r
0M1, r
0M2, E
0M1, and E
0M2 for the two different M sites in orthopyroxene according to the lattice strain model and calculated the intracrystalline
distribution between M1 and M2. Our data indicate extreme intracrystalline fractionation for most elements in orthopyroxene;
for the divalent cations D
i
M2−M1 varies by three orders of magnitude between D
CoM2−M1 = 0.00098–0.00919 and D
BaM2−M1 = 2.3–28. Trivalent cations Al and Cr almost exclusively substitute on M1 while the other trivalent cations substitute on
M2; D
LaM2−M1 reaches extreme values between 6.5 × 107 and 1.4 × 1016. Tetravalent cations Ti, Hf, and Zr almost exclusively substitute on M1 while U and Th exclusively substitute on M2. Our
new comprehensive data set can be used for polybaric-polythermal melting models along the Earth’s mantle solidus.
Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users. 相似文献
18.
Jin Li Suo‐han Tang Xiang‐kun Zhu Zhi‐hong Li Shi‐Zhen Li Bin Yan Yue Wang Jian Sun Yao Shi Aiguo Dong Nick S. Belshaw Xingchao Zhang Sheng‐ao Liu Ji‐hua Liu Deli Wang Shao‐yong Jiang KeJun Hou Anthony S. Cohen 《Geostandards and Geoanalytical Research》2019,43(1):163-175
Iron, Cu and Zn stable isotope systems are applied in constraining a variety of geochemical and environmental processes. Secondary reference materials have been developed by the Institute of Geology, Chinese Academy of Geological Sciences (CAGS), in collaboration with other participating laboratories, comprising three solutions (CAGS‐Fe, CAGS‐Cu and CAGS‐Zn) and one basalt (CAGS‐Basalt). These materials exhibit sufficient homogeneity and stability for application in Fe, Cu and Zn isotopic ratio determinations. Reference values were determined by inter‐laboratory analytical comparisons involving up to eight participating laboratories employing MC‐ICP‐MS techniques, based on the unweighted means of submitted results. Isotopic compositions are reported in per mil notation, based on reference materials IRMM‐014 for Fe, NIST SRM 976 for Cu and IRMM‐3702 for Zn. Respective reference values of CAGS‐Fe, CAGS‐Cu and CAGS‐Zn solutions are as follows: δ56Fe = 0.83 ± 0.07 and δ57Fe = 1.20 ± 0.13, δ65Cu = 0.57 ± 0.06, and δ66Zn = ?0.79 ± 0.12 and δ68Zn = ?1.65 ± 0.24, respectively. Those of CAGS‐Basalt are δ56Fe = 0.15 ± 0.07, δ57Fe = 0.22 ± 0.10, δ65Cu = 0.12 ± 0.08, δ66Zn = 0.17 ± 0.13, and δ68Zn = 0.34 ± 0.26 (2s). 相似文献
19.
Calculated Phase Relations in High-Pressure Metapelites in the System NKFMASH (Na2O-K2O-FeO-MgO-Al2O3-SiO2-H2O) 总被引：6，自引：0，他引：6
Using an internally consistent thermodynamic dataset and updatedmodels of activity–composition relation for solid solutions,petrogenetic grids in the system NKFMASH (Na2O–K2O–FeO–MgO–Al2O3–SiO2–H2O)and the subsystems NKMASH and NKFASH have been calculated withthe software THERMOCALC 3.1 in the P–T range 5–36kbar and 400–810°C, involving garnet, chloritoid,biotite, carpholite, talc, chlorite, kyanite/sillimanite, staurolite,phengite, paragonite, albite, glaucophane, jadeite, with quartz/coesiteand H2O in excess. These grids, together with calculated AFMcompatibility diagrams and P–T pseudosections, are shownto be powerful tools for delineating the phase equilibria andP–T conditions of Na-bearing pelitic assemblages for avariety of bulk compositions from high-P terranes around theworld. These calculated equilibria are in good agreement withpetrological studies. Moreover, contours of the calculated phengiteSi isopleths in P–T pseudosections for different bulkcompositions confirm that phengite barometry is highly dependenton mineral assemblage. KEY WORDS: phase relations; HP metapelite; NKFMASH; THERMOCALC; phengite geobarometry 相似文献
20.
Multivariate statistical analysis has been used for detailed examination of the relationship between the magnetic properties of Xuzhou urban topsoil, for example concentration-dependent properties (mass magnetic susceptibility (χ), susceptibility of anhysteretic remanent magnetization (χ
ARM), saturation isothermal remanent magnetization (SIRM), soft remanent magnetization (SOFT), and frequency-dependent magnetic susceptibility (χ
FD)) and feature-dependent properties (S
−100 mT ratio, SIRM/χ ratio and F
300 mT ratio), and the concentrations of metals (Ti, Fe, Cr, Al, Ga, Pb, Sc, Ba, Li, Cd, Be, Co, Cu, Mn, Ni, V, Zn, Mo, Pt, Pd, Au, As, Sb, Se, Hg, Bi, Ag, and Sn), S, and Br in the soil. The results show that SIRM/χ ratios correlate best with the heavy metals (Hg, Cr, Sb, As, and Bi) which are mainly derived from coal-combustion emissions whereas χ
FD correlates best with the metals (Al, Ti, V, Be, Co, Ga, Mn, and Li) which principally originate from soil parents. Concentration-dependent magnetic properties (χ
ARM, χ, SIRM, and SOFT) correlate well with elements (Se, Pb, Cu, Zn, Fe, Ag, Sc, Ba, Mo, Br, S, Cd, Ni, etc.) which are mainly derived from road-traffic emissions. For the same chemical element, χ
ARM, SIRM, and SOFT values are frequently better correlated than χ values, and χ
ARM values are the best indicators of the concentrations of these elements associated with traffic emissions in this study area. In addition, S
−100 mT ratios significantly correlate positively with Se, Sc, Pb, Cu, Zn, Mo, and S whereas F
300 mT ratios only correlate positively with Pt and negatively with Fe. These results confirm the suitability of different magnetic properties for characterizing the concentrations of heavy metals, S, and Br in Xuzhou urban topsoil. 相似文献