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多接收等离子质谱（MC-ICP-MS )测定Mg同位素初步研究 总被引：3，自引：3，他引：3
常量元素Mg的同位素比值，应用在地球化学上有重要意义。笔者采用“样品-标准”交叉技术，以国际标准SRM980,AIdrich, Romil和实验室标准GSB作为实验材料，探讨浓度和基质效应影响，尝试建立高精度多接收等离子质谱(MC-ICP-MS)测定Mg同位素方法。相对于国际标准物质SRM980，本研究测得的国际标准物质Aldrich的δ26Mg和δ25Mg值分别为（2.64±0.15)‰(2σ）和（1.34±0.09)‰(2σ); Romil的δ26Mg和δ25Mg值分别为（2.46±0.15)‰(2σ）和（1.27±0.08)%(2σ)；国土资源部同位素地质重点实验室的实验室标准GSB的δ26Mg和δ25Mg值分别为（4.05±0.03)‰(2σ)和(2.05±0.03)‰(2σ)。 相似文献
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本文报道了内蒙古狼山成矿带内两个最大的铅锌多金属硫化物矿床——东升庙矿床和炭窑口矿床中黄铁矿、黄铜矿单矿物的铁同位素研究结果。东升庙矿床绢云石墨片岩中不规则状黄铁矿的铁同位素组成δ~(56)Fe_(-IRMM)值在+0.04‰~+1.11‰之间,呈现铁的重同位素富集,指示了海水中的铁以氧化态沉淀并在成岩期转化成黄铁矿的矿化过程。东升庙和炭窑口矿床富硫化物矿石中黄铁矿和黄铜矿的铁同位素组成δ~(56)Fe_(-IRMM)值的变化范围为-1.33‰~+0.08‰,具有热液成矿特征,指示金属成矿物质来源于热液流体。另外,绢云石墨片岩中脉状黄铁矿的铁同位素组成δ~(56)Fe_(-IRMM)值的变化范围为-0.39‰~-0.04‰,处于矿石黄铁矿和围岩不规则状黄铁矿之间,指示脉状黄铁矿是热液矿化的产物,并在成矿过程中混入了围岩中早先形成的富集铁的重同位素的黄铁矿。绢云石墨片岩中广泛发育的不规则状黄铁矿与赋存在绢云石墨片岩中的富硫化物矿体具有完全不同的铁同位素组成,指示热液活动对不规则状黄铁矿没有明显成矿物质贡献,因此同沉积热液活动成矿的可能性不大。结合赋存在白云石大理岩中硫化物矿体的顶、底部常见硅化的白云石大理岩角砾,本文提出后生矿化是东升庙多金属硫化物矿体的主要成矿方式。另外,东升庙矿床和炭窑口矿床的矿石硫化物具有相似的铁同位素组成特征,指示两者的成矿物质来源具有相似性。 相似文献
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Ti separation was achieved by ion-exchange chromatography using Bio-Rad AG 1-X8 anion-exchange and DGA resins. For high-Fe/Ti and high-Mg/Ti igneous samples, a three-column procedure was required, whereas a two-column procedure was used for low-Fe/Ti and low-Mg/Ti igneous samples. The Ti isotopes were analysed by MC-ICP-MS, and instrumental mass bias was corrected using a 47Ti-49Ti double-spike technique. The 47Ti-49Ti double-spike and SRM 3162a were calibrated using SRM 979-Cr, certificated value 53Cr/52Crtrue = 0.11339. Isobaric interference was evaluated by analysing Alfa-Ti doped with Na, Mg, Ca, and Mo, and results indicate that high concentrations of Na and Mg have no significant effect on Ti isotope analyses; however, Ca and Mo interferences lead to erroneous δ49/47Ti values when Ca/Ti and Mo/Ti ratios exceed 0.01 and 0.1, respectively. Titanium isotopic compositions were determined for 12 igneous reference materials, BCR-2, BHVO-2, GBW07105, AGV-1, AGV-2, W-2, GBW07123, GBW07126, GBW07127, GBW07101, JP-1, and DTS-2b. Samples yield δ49/47Ti (‰) of ?0.035 ± 0.022, ?0.038 ± 0.031, 0.031 ± 0.022, 0.059 ± 0.038, 0.044 ± 0.037, 0.000 ± 0.015, 0.154 ± 0.044, ?0.044 ± 0.018, 0.010 ± 0.022, 0.064 ± 0.043, 0.169 ± 0.034, and ?0.047 ± 0.025 (relative to OL-Ti, ±2SD), respectively; of which isotopic compositions of DTS-2b, JP-1, GBW07101, GBW07105, GBW07123, GBW07126, and GBW07127 are reported for the first time. Standard Alfa-Ti was analysed repeatedly over a ten-month period, indicating a reproducibility of ±0.047 (2SD) for δ49/47Ti, similar to the precisions obtained for geochemical reference materials. 相似文献
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Xinmiao Zhao Hongfu Zhang Xiangkun Zhu Suohan Tang Yanjie Tang 《Contributions to Mineralogy and Petrology》2010,160(1):15-14
Iron isotopes, together with mineral elemental compositions of spinel peridotite xenoliths and clinopyroxenites from Hannuoba
and Hebi Cenozoic alkaline basalts, were analyzed to investigate iron isotopic features of the lithospheric mantle beneath
the North China Craton. The results show that the Hannuoba spinel peridotite xenoliths have small but distinguishable Fe isotopic
variations. Overall variations in δ57Fe are in a range of −0.25 to 0.14‰ for olivine, −0.17 to 0.17‰ for orthopyroxene, −0.21 to 0.27‰ for clinopyroxene, and −0.16
to 0.26‰ for spinel, respectively. Clinopyroxene has the heaviest iron isotopic ratio and olivine the lightest within individual
sample. No clear linear relationships between the mineral pairs on “δ-δ” plot suggest that iron isotopes of mineral separates
analyzed have been affected largely by some open system processes. The broadly negative correlations between mineral iron
isotopes and metasomatic indexes such as spinel Cr#, (La/Yb)N ratios of clinopyroxenes suggest that iron isotopic variations in different minerals and peridotites were probably produced
by mantle metasomatism. The Hebi phlogopite-bearing lherzolite, which is significantly modified by metasomatic events, appears
to be much heavier isotopically than clinopyroxene-poor lherzolite. This study further confirms previous conclusions that
the lithospheric mantle has distinguishable and heterogeneous iron isotopic variations at the xenoliths scale. Mantle metasomatism
is the most likely cause for the iron isotope variations in mantle peridotites. 相似文献
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Iron isotope variations in spinel peridotite xenoliths from North China Craton: implications for mantle metasomatism 总被引：2，自引：1，他引：1
Xinmiao Zhao Hongfu Zhang Xiangkun Zhu Suohan Tang Yanjie Tang 《Contributions to Mineralogy and Petrology》2010,160(1):1-14
Iron isotopes, together with mineral elemental compositions of spinel peridotite xenoliths and clinopyroxenites from Hannuoba and Hebi Cenozoic alkaline basalts, were analyzed to investigate iron isotopic features of the lithospheric mantle beneath the North China Craton. The results show that the Hannuoba spinel peridotite xenoliths have small but distinguishable Fe isotopic variations. Overall variations in δ57Fe are in a range of ?0.25 to 0.14‰ for olivine, ?0.17 to 0.17‰ for orthopyroxene, ?0.21 to 0.27‰ for clinopyroxene, and ?0.16 to 0.26‰ for spinel, respectively. Clinopyroxene has the heaviest iron isotopic ratio and olivine the lightest within individual sample. No clear linear relationships between the mineral pairs on “δ-δ” plot suggest that iron isotopes of mineral separates analyzed have been affected largely by some open system processes. The broadly negative correlations between mineral iron isotopes and metasomatic indexes such as spinel Cr#, (La/Yb)N ratios of clinopyroxenes suggest that iron isotopic variations in different minerals and peridotites were probably produced by mantle metasomatism. The Hebi phlogopite-bearing lherzolite, which is significantly modified by metasomatic events, appears to be much heavier isotopically than clinopyroxene-poor lherzolite. This study further confirms previous conclusions that the lithospheric mantle has distinguishable and heterogeneous iron isotopic variations at the xenoliths scale. Mantle metasomatism is the most likely cause for the iron isotope variations in mantle peridotites. 相似文献
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本文初步报道了长江中下游铜陵矿集区内冬瓜山斑岩-矽卡岩型Cu-Au矿中硫化物、石英闪长岩体和赋矿围岩的Cu同位素组成特征。其中,硫化物的δ65Cu变化范围为-0.54‰~0.95‰,变化范围较大,可达1.5‰,表明高温成矿体系下铜同位素发生分馏,铜同位素具有示踪高温成矿作用过程的潜力。不同空间位置的黄铜矿的铜同位素组成呈现出空间分带特征,表现为从岩体→斑岩型矿体→近岩体矽卡岩→矽卡岩型矿体,随着远离岩体,黄铜矿的铜同位素组成逐渐变重。导致斑岩-矽卡岩型矿床铜同位素出现空间分带的主要原因是矿化过程中铜同位素发生分馏。并且,对于冬瓜山矿床来讲,导致铜同位素组成空间分带的分馏不是发生在Cu在气-液两相之间分配的过程中,而是发生在硫化物从流体中沉淀出来的过程中。在硫化物的沉淀过程中,铜的重同位素优先在流体中富集,轻同位素在沉淀中富集,随着流体向外迁移,硫化物沉淀的进行,残余热液流体会逐渐富集铜的重同位素。硫化物的铜同位素组成可以用来反演和指示成矿流体的迁移方向。 相似文献
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铜陵矿集区冬瓜山矿床斑岩-矽卡岩型矿床成矿作用过程中的Cu同位素地球化学行为初步研究 总被引：3，自引：0，他引：3
本文报道了长江中下游铜陵矿集区内冬瓜山斑岩-矽卡岩型Cu-Au矿床中硫化物、石英闪长岩体和赋矿围岩的Cu同位素组成特征.其中,硫化物的δ65 Cu变化范围为-0.54‰～0.95‰,变化范围较大,达1.5‰,表明高温成矿体系下铜同位素发生分馏,铜同位素具有示踪高温成矿作用过程的潜力.不同空间位置的黄铜矿的铜同位素组成呈现出空间分带特征,表现为从岩体和斑岩型矿体→近岩体矽卡岩→矽卡岩型矿体,随着远离岩体,黄铜矿的铜同位素组成逐渐变重.导致斑岩-矽卡岩型矿床铜同位素出现空间分带的主要原因是矿化过程中铜同位素发生分馏.并且,对于冬瓜山矿床来讲,导致铜同位素组成空间分带的分馏不是发生在Cu在气-液两相之间分配的过程中,而是发生在硫化物从流体中沉淀出来的过程中.在硫化物的沉淀过程中,铜的重同位素优先在流体中富集,轻同位素在沉淀中富集,随着流体向外迁移,硫化物沉淀的进行,残余热液流体会逐渐富集铜的重同位素.硫化物的铜同位素组成可以用来反演和指示成矿流体的迁移方向. 相似文献
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Haitaite-(La), (La, Ce)(U4+, U6+, Fe2+)(Fe3+, Al)2(Ti, Fe2+, Fe3+)18O38, is a new member of the crichtonite group. It is named after the Haita Village in the Miyi County of Sichuan Province, China, where the mineral was discovered. The mineral occurs as black opaque centimeter-sized aggregates in the external contact zone between the Neoproterozoic (~800 Ma) alkali feldspar granite and the Mesoproterozoic (~1700 Ma) micaschist. In the studied sample, haitaite-(La) is associated with other minerals, including ilmenite, magnetite, rutile, zircon, brannerite and uraninite. The new mineral is a black, metallic phase and has a Mohs hardness of 6, with a density of 4.99 g/cm3 (calculated) and 5.03 g/cm3 (measured). Haitaite-(La) is opaque in transmitted light and grayish-white under reflected light, with a reflectivity between 22.5% and 16.42% in the 400–700 nm band (SiC, in the air). The compositions of the mineral were measured by EPMA, the U4+/U6+ ratio was determined by X-ray photoelectron spectroscopy and the Fe2+/Fe3+ ratio was determined by M?ssbauer spectroscopy. Haitaite-(La) is trigonal, belongs to R3ˉ and has unit-cell parameters a = 10.3678(5) ?, c = 20.8390(11) ?, V = 1939.9(2) ?3, Z = 3. The crystalline structure is composed of octahedra with 9 layers of close-packed octahedra (M1, M3, M4, M5), tetrahedra (M2) and contains large 12-coordinated M0 sites. 相似文献