新疆绿色电气石颜色成因研究

新疆绿色电气石颜色成因比较特殊,为了更好地了解其颜色的形成,主要采用化学分析、吸收光谱、穆斯堡尔谱等测试手段对绿色电气石颜色成因进行研究。化学分析结果显示每个样品中均含有少量不同过渡元素离子,如Fe2 、Ti4 、Cr3 等,影响着绿色的形成;利用吸收光谱测试方法确定了致色离子的吸收带位置及主要离子的种类、价态,并根据化学成分计算出相应的化学式,利用穆斯堡尔谱确定了铁离子在晶体中的占位。综合运用上述测试方法,确定了绿色电气石的颜色成因。     

Oxydation expérimentale de Fe-tourmalines et corrélation avec une déprotonation des groupes hydroxyleAnnealing in oxidising conditions of Fe-tourmalines and correlated deprotonation of OH groups

Annealing at 400?T?600 °C (40?P?60 MPa and HM buffer-controlled f(O₂)) of tourmalines synthesised at the same T and P with NNO buffer induces an oxidation of Fe²⁺ into Fe³⁺ in some Y sites only (Mössbauer Spectroscopy data). Annealing in the same conditions of natural tourmalines is consistent with these results. FTIR spectroscopy shows that oxidation of Fe²⁺ into Fe³⁺ is charge-balanced by deprotonation of the external OH₍₃₎ groups. To cite this article: Y. Fuchs et al., C. R. Geoscience 334 (2002) 245–249.     

甘肃南祁连余石山地区变粒岩原岩恢复

余石山地区位于南祁连西南端,处在祁连—柴达木—阿尔金地块的交汇部位,构造复杂。长城纪熬油沟组中的变粒岩,由于变质程度较深,以及后期构造的影响,原岩的特征难以辨别。本文通过岩石地球化学方法,对该区变粒岩及其原岩进行了研究,结果显示其原岩为中酸性岩浆岩,结合高场强元素特征和高的碱含量,确定其原岩为正长岩类。     

熔融制样-X射线荧光光谱法测定电气石中12种主次量元素

电气石是一类含硼的铝硅酸盐矿物,化学成分复杂、化学稳定性强,不易湿法分解,B_2O_3含量较高,导致其主次量元素的同时测定存在一定困难。本文采用熔融法制样,建立了X射线荧光光谱法测定电气石Na_2O、MgO、Al_2O_3、SiO_2、P_2O_5、K_2O、CaO、TiO_2、V_2O_5、Cr_2O_3、MnO、TFe_2O_3等主次量元素的分析方法。样品与四硼酸锂-偏硼酸锂-氟化锂(质量比为4.5∶1∶0.4)混合熔剂的稀释比例为1∶10,消除了粒度效应和矿物效应;在缺少电气石标准物质的情况下,选择土壤、水系沉积物及多种类型的地质标准物质绘制校准曲线,利用含量与电气石类似的标准物质验证准确度,测定结果的相对标准偏差小于4.2%。采用所建方法测定四种不同类型电气石实际样品,测定值与经典化学法基本吻合。本方法解决了电气石不易湿法分解和硼的干扰问题,测定结果准确可靠,与其他方法相比操作简便,分析周期短。     

硅硼镁铝矿－柱晶石－电气石组合在南极的发现

硅硼镁铝矿、柱晶石和电气石组合产于东南极拉斯曼丘陵，三种矿物相互接触并表现出特定的顺序：电气石（Ｔｒｎ１）→硅硼镁铝矿→电气石（Ｔｒｎ２）→柱晶石→电气石（Ｔｒｎ３），表明其产出是受Ｂ２Ｏ３、Ｈ２Ｏ活度的时间演化而不是空间变化所控制。这一组合的出现对于变质作用环境及过程中组分性质是一个很好的限定     

齐大山铁矿黑云变粒岩单锆石年龄及意义

齐大山特大型鞍山式铁矿的成矿时代，以往都是根据铁矿的构造和建造特征，以及与铁矿伴生的花岗岩类岩体的同位素年龄数据间接推断的。本文最近获得了该铁矿的黑云变粒岩中，单颗粒锆石Ｕ－Ｐｂ同位素年龄为（２５３３±５３）×１０￣６ａ。这是迄今为止研究该矿床成矿时代较为可靠的直接测年数据。     

福建南平花岗伟晶岩中的电气石研究

电气石是南平伟晶岩和围岩中分布广泛的一种副矿物,根据化学成分,它们属于镁铁锂电气石亚族,其端员为铁(黑)电气石、镁电气石和锂电气石,其间还有一系列过渡矿物。南平伟晶岩中除未发现端员锂电气石外,其他端员及过渡系列电气石均十分发育,这在国内外同类伟晶岩中十分少见。不同成分电气石分布于不同类型伟晶岩及同一伟晶岩分异演化的不同阶段。本文在对电气石的化学成分、物理性质、产状等较详阐述基础上,对它们的演变规律及形成环境进行了讨论,这对于探讨南平伟晶岩的形成及寻找稀有金属伟晶岩有重要意义。     

Mineral Geochemical Compositions of Tourmalines and Their Significance in the Gejiu Tin Polymetallic Deposits, Yunnan, China

Abstract: The Gejiu tin polymetallic deposits are located in the southeastern part of Yunnan Province in China. A detailed electronic microprobe study has been carried out to document geochemical compositions of tourmalines from the deposits. The results indicate a systematic change of mineral geochemical compositions, which might be used as a mineral geochemical tracer for post-magmatic hydrothermal fluid, basin fluid and their mixture. The tourmalines from granite are schorl with Fe/(Fe+Mg) ratios of 0.912-1.00 and Na/(Na+Ca) ratios of 0.892-0.981. Tourmalines as an inclusion in quartz from the ore bodies are dravite with Fe/(Fe+Mg) ratios of 0.212-0.519 and Na/ (Na+Ca) ratios of 0.786-0.997. Tourmalines from the country rocks are dravite with Fe/(Fe+Mg) ratios of 0.313-0.337 and Na/(Na+Ca) ratio of 0.599-0.723. Tourmalines from cassiterite-tourmaline veins that occur in crannies within the country rocks show distinct optical zoning with alternate occurrence of dravite and schorl, Fe/(Fe+Mg)=0.374-0.843, Na/(Na+Ca)=0.538-0.987. It suggests that schorl in granite and dravite in carbonatite are related to magmatic fluid and basin fluid respectively. When magmatic fluid rose up and entered into crannies of the country rocks, consisting mainly of carbonatite, basin fluid would be constantly added to the magmatic fluid. The two types of fluid were mixed in structural crannies of the sedimentary basin accompanied with periodic geochemical oscillations to form material records in chemical composition zonings of tourmalines.     

电气石矿物吸附铜离子试验研究

本文研究了电气石的单晶、电气石微粉对Cu2＋的吸附作用,试验表明：电气石单晶体表面存在着以C轴为两极的静电场,该静电场对Cu2＋的吸附作用效果明显。制备的电气石微粒越细,吸附效果越好。电气石的电场效应使得它在治理污水中Cu2＋污染具有广阔的前景。     

Development and Re‐Evaluation of Tourmaline Reference Materials for In Situ Measurement of Boron δ Values by Secondary Ion Mass Spectrometry

Six tourmaline samples were investigated as potential reference materials (RMs) for boron isotope measurement by secondary ion mass spectrometry (SIMS). The tourmaline samples are chemically homogeneous and cover a compositional range of tourmaline supergroup minerals (primarily Fe, Mg and Li end‐members). Additionally, they have homogeneous boron delta values with intermediate precision values during SIMS analyses of less than 0.6‰ (2s). These samples were compared with four established tourmaline RMs, that is, schorl IAEA‐B‐4 and three Harvard tourmalines (schorl HS#112566, dravite HS#108796 and elbaite HS#98144). They were re‐evaluated for their major element and boron delta values using the same measurement procedure as the new tourmaline samples investigated. A discrepancy of about 1.5‰ in δ¹¹B was found between the previously published reference values for established RMs and the values determined in this study. Significant instrumental mass fractionation (IMF) of up to 8‰ in δ¹¹B was observed for schorl–dravite–elbaite solid solutions during SIMS analysis. Using the new reference values determined in this study, the IMF of the ten tourmaline samples can be modelled by a linear combination of the chemical parameters FeO + MnO, SiO₂ and F. The new tourmaline RMs, together with the four established RMs, extend the boron isotope analysis of tourmaline towards the Mg‐ and Al‐rich compositional range. Consequently, the in situ boron isotope ratio of many natural tourmalines can now be determined with an uncertainty of less than 0.8‰ (2s).