Thermal equation of state of natural tourmaline at high pressure and temperature     

Jingui Xu  Yunqian Kuang  Bo Zhang  Yonggang Liu  Dawei Fan  Xiaodong Li  Hongsen Xie 《Physics and Chemistry of Minerals》2016,43(5):315-326

Synchrotron-based in situ angle-dispersive X-ray diffraction experiments were conducted on a natural uvite-dominated tourmaline sample by using an external-heating diamond anvil cell at simultaneously high pressures and temperatures up to 18 GPa and 723 K, respectively. The angle-dispersive X-ray diffraction data reveal no indication of a structural phase transition over the P–T range of the current experiment in this study. The pressure–volume–temperature data were fitted by the high-temperature Birch–Murnaghan equation of state. Isothermal bulk modulus of K ₀ = 96.6 (9) GPa, pressure derivative of the bulk modulus of \(K_{0}^{\prime } = 12.5 \;(4)\), thermal expansion coefficient of α ₀ = 4.39 (27) × 10^?5 K^?1 and temperature derivative of the bulk modulus (?K/?T) _P  = ?0.009 (6) GPa K^?1 were obtained. The axial thermoelastic properties were also obtained with K _a0 = 139 (2) GPa, \(K_{a0}^{\prime }\) = 11.5 (7) and α _a0 = 1.00 (11) × 10^?5 K^?1 for the a-axis, and K _c0 = 59 (1) GPa, \(K_{c0}^{\prime }\) = 11.4 (5) and α _c0 = 2.41 (24) × 10^?5 K^?1 for the c-axis. Both of axial compression and thermal expansion exhibit large anisotropic behavior. Thermoelastic parameters of tourmaline in this study were also compared with that of the other two ring silicates of beryl and cordierite.  相似文献   

Ionic conductivity in gem-quality single-crystal alkali feldspar from the Eifel: temperature,orientation and composition dependence     

Hamid El Maanaoui  Fabian Wilangowski  Aditya Maheshwari  Hans-Dieter Wiemhöfer  Rainer Abart  Nicolaas A. Stolwijk 《Physics and Chemistry of Minerals》2016,43(5):327-340

We measured the ion conductivity of single-crystal alkali feldspar originating from two different locations in the Eifel/Germany, named Volkesfeld and Rockeskyller sanidine and having potassium site fractions \(C_\mathrm{K}\) of 0.83 and 0.71, respectively. The dc conductivities resulting from electrochemical impedance spectroscopy over the temperature range of 300–900 \(^{\circ }\hbox {C}\) show a weak composition dependence but pronounced differences between the b-direction [\(\perp (010)\)] and \(c^{*}\)-direction [\(\perp (001)\)] of the monoclinic feldspar structure. Conductivity activation energies obtained from the observed linear Arrhenius plots are close to 1.2 eV in all cases, which is closely similar to the activation energies of the \(^{22}\mathrm{Na}\) tracer diffusivity in the same crystals. Taking into account literature data on K tracer diffusion and diffusion correlation effects, the present results point to a predominance of the interstitialcy mechanism over the vacancy mechanism in mass and charge transport on the alkali sublattice in potassium-rich alkali feldspar.  相似文献   

Phase relation of CaSO<Subscript>4</Subscript> at high pressure and temperature up to 90 GPa and 2300 K     

Taku Fujii  Hiroaki Ohfuji  Toru Inoue 《Physics and Chemistry of Minerals》2016,43(5):353-361

Calcium sulfate (CaSO₄), one of the major sulfate minerals in the Earth’s crust, is expected to play a major role in sulfur recycling into the deep mantle. Here, we investigated the crystal structure and phase relation of CaSO₄ up to ~90 GPa and 2300 K through a series of high-pressure experiments combined with in situ X-ray diffraction. CaSO₄ forms three thermodynamically stable polymorphs: anhydrite (stable below 3 GPa), monazite-type phase (stable between 3 and ~13 GPa) and barite-type phase (stable up to at least 93 GPa). Anhydrite to monazite-type phase transition is induced by pressure even at room temperature, while monazite- to barite-type transition requires heating at least to 1500 K at ~20 GPa. The barite-type phase cannot always be quenched from high temperature and is distorted to metastable AgMnO₄-type structure or another modified barite structure depending on pressure. We obtained the pressure–volume data and density of anhydrite, monazite- and barite-type phases and found that their densities are lower than those calculated from the PREM model in the studied P–T conditions. This suggests that CaSO₄ is gravitationally unstable in the mantle and fluid/melt phase into which sulfur dissolves and/or sulfate–sulfide speciation may play a major role in the sulfur recycling into the deep Earth.  相似文献   

In situ high-temperature X-ray diffraction and spectroscopic study of fibroferrite,FeOH(SO<Subscript>4</Subscript>)·5H<Subscript>2</Subscript>O     

Gennaro Ventruti  Giancarlo Della Ventura  Nicola Corriero  Daniele Malferrari  Alessandro F. Gualtieri  Umberto Susta  Maria Lacalamita  Emanuela Schingaro 《Physics and Chemistry of Minerals》2016,43(8):587-595

The thermal dehydration process of fibroferrite, FeOH(SO₄)·5H₂O, a secondary iron-bearing hydrous sulfate, was investigated by in situ high-temperature synchrotron X-ray powder diffraction (HT-XRPD), in situ high-temperature Fourier transform infrared spectroscopy (HT-FTIR) and thermal analysis (TGA-DTA) combined with evolved gas mass spectrometry. The data analysis allowed the determination of the stability fields and the reaction paths for this mineral as well as characterization of its high-temperature products. Five main endothermic peaks are observed in the DTA curve collected from room T up to 800 °C. Mass spectrometry of gases evolved during thermogravimetric analysis confirms that the first four mass loss steps are due to water emission, while the fifth is due to a dehydroxylation process; the final step is due to the decomposition of the remaining sulfate ion. The temperature behavior of the different phases occurring during the heating process was analyzed, and the induced structural changes are discussed. In particular, the crystal structure of a new phase, FeOH(SO₄)·4H₂O, appearing at about 80 °C due to release of one interstitial H₂O molecule, was solved by ab initio real-space and reciprocal-space methods. This study contributes to further understanding of the dehydration mechanism and thermal stability of secondary sulfate minerals.  相似文献   

Anisotropic mechanical properties of zircon and the effect of radiation damage     

Tobias Beirau  William D. Nix  Ulrich Bismayer  Lynn A. Boatner  Scott G. Isaacson  Rodney C. Ewing 《Physics and Chemistry of Minerals》2016,43(9):627-638

This study provides new insights into the relationship between radiation-dose-dependent structural damage due to natural U and Th impurities and the anisotropic mechanical properties (Poisson’s ratio, elastic modulus and hardness) of zircon. Natural zircon samples from Sri Lanka (see Muarakami et al. in Am Mineral 76:1510–1532, 1991) and synthetic samples, covering a dose range of zero up to 6.8 × 10¹⁸ α-decays/g, have been studied by nanoindentation. Measurements along the [100] crystallographic direction and calculations, based on elastic stiffness constants determined by Özkan (J Appl Phys 47:4772–4779, 1976), revealed a general radiation-induced decrease in stiffness (~54 %) and hardness (~48 %) and an increase in the Poisson’s ratio (~54 %) with increasing dose. Additional indentations on selected samples along the [001] allowed one to follow the amorphization process to the point that the mechanical properties are isotropic. This work shows that the radiation-dose-dependent changes of the mechanical properties of zircon can be directly correlated with the amorphous fraction as determined by previous investigations with local and global probes (Ríos et al. in J Phys Condens Matter 12:2401–2412, 2000a; Farnan and Salje in J Appl Phys 89:2084–2090, 2001; Zhang and Salje in J Phys Condens Matter 13:3057–3071, 2001). The excellent agreement, revealed by the different methods, indicates a large influence of structural and even local phenomena on the macroscopic mechanical properties. Therefore, this study indicates the importance of acquiring better knowledge about the mechanical long-term stability of radiation-damaged materials.  相似文献   

南美Oriente盆地北部海绿石砂岩油藏特征及成藏规律          下载免费PDF全文

阳孝法  谢寅符  张志伟  陈和平  马中振  周玉冰  王丹丹  刘亚明  贺正军  赵永斌 《地质科学》2016,(1):189-203

南美厄瓜多尔Oriente盆地斜坡带发育的白垩系Napo组高伽马特征的UT海绿石砂岩段是成熟探区新发现的隐蔽含油层段。本文分析了海绿石砂岩储层的矿物组成、孔隙结构、成岩作用、物性特点,并结合烃源岩评价与石油空间分布探讨海绿石砂岩油藏的成藏特征。海绿石粘土矿物以颗粒形式存在,与石英共同构成海绿石砂岩的颗粒组分,海绿石砂岩的孔隙结构具有双峰特征,束缚水含量高,属于中-低孔、中-低渗储层类型,孔隙类型主要是剩余粒间孔。海绿石砂岩储层中石英次生加大属Ⅱ级,长石碎屑颗粒发生溶蚀作用,含铁碳酸盐类胶结物发育,结合泥岩低的I/S混层比和高的最高峰温值T_max,指示海绿石砂岩层段属于中成岩阶段A期的产物。与海绿石砂岩油藏紧邻的大面积分布的Ⅱ₁腐泥型成熟烃源岩就是缓翼斜坡带的生烃中心,大面积连续发育的海绿石砂岩与之构成优越的源储组合,有利于上生下储式成藏。海绿石砂岩油藏表现为近源性、成藏晚期性等特点,规模发育的海绿石砂岩储层得以成藏的主要运聚机制是体积流和扩散流运聚机制。这对盆地其它油区同类油藏的发现具有重要的借鉴意义。  相似文献   

香港世界地质公园晚侏罗世荔枝庄组岩石组合及其成岩地质过程解析     

姜杨  杨家明  杨祝良  沈加林  马雪  陈羽岚  钱迈平  邢光福  余明刚  段政 《地质论评》2016,62(3):759-769

中国东南大陆晚侏罗世地层普遍缺失,仅零星见于个别地区,香港新界东北的荔枝庄组即为其一。荔枝庄组出露于香港世界地质公园沉积岩园区的荔枝庄地区,自下往上由火山岩—沉积岩—火山岩组合而成,沉积岩中发育大型包卷层理和滑塌构造等典型沉积构造,是香港地区最具代表性的晚侏罗世火山—沉积岩系。通过实测地层剖面研究,确定其成岩过程大体上可划分为早期普林尼式火山爆发、中期破火山口湖相沉积和晚期普林尼式火山爆发三个阶段,以湖相沉积作用为主、火山喷发作用为辅;受晚期火山岩浆活动的影响,沉积岩层普遍发生硅化或炭化。荔枝庄组独特的岩石组合与形成的古地理环境,为探讨中国东南大陆中生代火山活动—沉积作用方式与成岩过程,提供了难得的研究实例。  相似文献   

西藏班公湖-怒江缝合带西段特提斯洋晚二叠世(Ca.252Ma)洋内俯冲的地球化学和年代学证据     

韦少港  宋扬  唐菊兴 《地质论评》2016,62(S1):194-196

多龙蛇绿混杂岩是班公湖-怒江蛇绿岩带的重要组成部分,位于西藏阿里地区改则县北西约120 km的多龙矿集区内,大地构造位置处于班公湖-怒江缝合带中西段,南羌塘板块南缘。多龙蛇绿混杂岩主要分布在多龙矿区中部及东北部。矿区中部蛇绿岩主要由辉长岩、辉绿(玢)岩、枕状玄武岩、气孔杏仁状玄武岩、玄武质岩屑凝灰岩及硅质岩等组成,东西向延伸约35 km,南北宽3~7 km,出露面积约180 km2;该蛇绿岩残片的组成单元(包括基性岩单元以及硅质岩单元等)多被构造肢解,整体表现为不规则透镜体,以构造岩片的形式断续分布于侏罗系次深海陆棚-盆地斜坡复陆碎屑岩-类复理石建造内的断层带中,构成典型的网结状构造。矿区东北部蛇绿岩主要由含铁斜方辉石橄榄蛇纹岩、玻基玄武岩、碳酸盐化角闪辉长岩、微纹层状硅质岩等组成,该蛇绿混杂岩带沿北西-南东向断裂展布,延伸约12 km,宽1~3 km,出露面积约30 km2;该蛇绿岩残片组成单元(包括超基性岩单元、基性岩单元以及硅质岩单元等)均呈构造岩片的形式产出在三叠系灰岩地层内的断层带中。  相似文献   

云南大红山地区铁、铜矿床类型及形成机理     

李锡康  程胜辉  朱多录  柏杨  孙鹏  郝学峰  李蓉 《地质论评》2016,62(S1):213-214

大红山地区是云南省重要矿集区之一,已发现大红山大型铁铜矿床及东么、底巴都、底戛母、河口、坝达等多个中小型铁铜矿床（点）,区内分布多个磁异常及化探异常,成矿地质条件优越。近年云南省三年地质找矿行动计划项目“云南省新平县大红山外围铁、铜矿资源普查”经过勘查在大红山外围东么、底巴都矿区圈定多个工业铁、铜矿体及超贫磁铁矿体,取得一定找矿新进展。本文根据近年工作中观察到的新现象、取得的新资料,结合前人研究成果,对大红山地区铁、铜矿床成因类型及形成机理进行探讨。  相似文献   

A Study on the Vibration Frequency of Blasting Excavation in Highly Stressed Rock Masses     

Jianhua Yang  Wenbo Lu  Qinghui Jiang  Chi Yao  Shuihua Jiang  Lin Tian 《Rock Mechanics and Rock Engineering》2016,49(7):2825-2843

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