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1.
R. Hellmann J.-M. Penisson R. L. Hervig J.-H. Thomassin M.-F. Abrioux 《Physics and Chemistry of Minerals》2003,30(4):192-197
Using an approach combining high-resolution and energy-filtered transmission electron microscopy (HRTEM and EFTEM), we have studied with Å to nm-spatial resolution the interfacial region that delimits the near-surface altered zone and non-altered labradorite feldspar after dissolution under acid pH conditions. The interface is characterized by extremely sharp and spatially coincident changes in structure and chemistry. The 500-nm-thick altered zone is depleted in interstitial cations (Ca, Na, K) and Al, a framework element, whereas it is enriched in H, O, and Si. Modeling H+-alkali interdiffusion within a 500-nm-thick altered zone shows that volume interdiffusion cannot reproduce the sharp chemical interfaces measured by EFTEM. Based on these new data, we propose that the near-surface altered zone is a result of interfacial dissolution-reprecipitation, and not of preferential leaching of cations and interdiffusion with H+. This implies an intrinsic dissolution process that is stoichiometric, where the breaking of bonds and release of interstitial cations and framework elements (Al, Si, and O) to solution occur contemporaneously at equal relative rates from the original fluid–mineral interface. 相似文献
2.
《Comptes Rendus Geoscience》2015,347(3):124-133
The organization of disordered carbons at the nanometer scale, or nanostructure, reveals very precisely their formation conditions, either in Nature or in the laboratory or in industry. Its study allows a better understanding of the properties of such solids. Only High-Resolution Transmission Electron Microscopy (HRTEM) allows a direct imaging of the nanostructure, whereas Raman microspectrometry provides quantitative but averaged structural data. Applications of the original coupling of Raman with HRTEM, especially in the fields of Energy and Environment, are numerous and promising. Two examples are given concerning the decontamination of irradiated nuclear graphite waste and detection of hydrocarbons trapped in oil and gas shales. Moreover, the study of wood carbonization led our team to propose a novel Raman-based paleothermometer. This approach finds an unexpected application in archeology (e.g., the study of fire marks in prehistoric caves). 相似文献
3.
Kerogen plays an important role in shale gas adsorption, desorption and diffusion. Therefore, it is necessary to characterize the molecular structure of kerogen. In this study, four kerogen samples were isolated from the organic-rich shale of the Longmaxi Formation. Raman spectroscopy was used to determine the maturity of these kerogen samples. High-resolution transmission electron microscopy (HRTEM), 13C nuclear magnetic resonance (13C NMR) , X-ray diffraction (XRD) and Fourier transform infrared (FT-IR) spectroscopy were conducted to characterize the molecular structure of the shale samples. The results demonstrate that VReqv of these kerogen samples vary from 2.3% to 2.8%, suggesting that all the kerogen samples are in the dry gas window. The macromolecular carbon skeleton of the Longmaxi Formation kerogen is mainly aromatic (fa’=0.56). In addition, the aromatic structural units are mainly composed of naphthalene (23%), anthracene (23%) and phenanthrene (29%). However, the aliphatic structure of the kerogen macromolecules is relatively low (fal*+falH=0.08), which is presumed to be distributed in the form of methyl and short aliphatic chains at the edge of the aromatic units. The oxygen-containing functional groups in the macromolecules are mainly present in the form of carbonyl groups (fac=0.23) and hydroxyl groups or ether groups (falO=0.13). The crystallite structural parameters of kerogen, including the stacking height (Lc=22.84 ?), average lateral size (La=29.29 ?) and interlayer spacing (d002=3.43 ?), are close to the aromatic structural parameters of anthracite or overmature kerogen. High-resolution transmission electron microscopy reveals that the aromatic structure is well oriented, and more than 65% of the diffractive aromatic layers are concentrated in the main direction. Due to the continuous deep burial, the longer aliphatic chains and oxygen-containing functional groups in the kerogen are substantially depleted. However, the ductility and stacking degree of the aromatic structure increases during thermal evolution. This study provides quantitative information on the molecular structure of kerogen samples based on multiple research methods, which may contribute to an improved understanding of the organic pores in black shale. 相似文献
4.
The microstructure of palygorskite from Longwang Mountain of Xuyu County, Jiangsu Province, was studied by energy dispersive X-ray analysis （EDX）, selected-area electron diffraction （SAED） and high-resolution transmission electron microscopy （HRTEM）. The average composition of the palygorskite studied is （Si7.38A10.62） （A10.96Fe^3＋ 0.62Mg2.86 0.56）Ca0.03K0.06O20（OH）2（OH2）4, which is rich in Mg. Several SAED patterns from a single crystal of palygorskite were obtained with different zone axes. The polymorphs （monoclinic and orthorhombic） are unequivocally distinguished by distant interplanar angles, even though they possess similar sets of d-values. High-resolution images of three principal zones （[010], [100] and [110]） were obtained. The lattice fringes on HRTEM images along [010] have spacings of 0.319 nm. These fringes are interpreted as periodic alterations of two tetrahedral （T） sheets and one octahedral （O） sheet （-TT-O-TT-O-）. We have directly observed trioctahedral and dioctahedral individual palygorskite particles along [100]. They are all presented as dark lines along [001], but the width of dark lines corresponding to trioctahedral crystals （0.913 nm） is twice that of the dioctahedral ones （0.456 nm）. This is because the trans.sites are occupied by cations in trioctahedral palygorskite. The width of dark lines along [110] is 1.024 nm, a bit thinner than the theoretical spacing （1.044 nm）. This is because water molecules quickly leave the structure upon the irradiation by the electron beam. 相似文献
5.
含金毒砂中晶格金的确定及其形成机理研究 总被引：7，自引：0，他引：7
利用电子探针(EPMA)和高分辨透射电子图像(HRTEM)分析技术,对湖南黄金洞金矿含金毒砂进行了背散射电子图像、X-射线面扫描、定量微区分析、线分析以及高分辨晶体结构观测等综合研究。结果表明,含金毒砂中没有发现纳米级乃至更小粒级的超显微包体金,毒砂晶格完整,无任何“异构体”,Au散布于整个毒砂颗粒中,以晶格金形式存在。此外,金含量在不同的生长环带中有显著变化,表明Au是在毒砂形成过程中进入其晶格的。金的加入导致毒砂晶体结构中(100)面网间距局部变宽,晶胞参数也发生了微弱变化,a轴变长。详细分析认为,Au主要是以Au~(3+)替代Fe~(3+)进入AsS~(3-)八面体空位中的,Eh值变化可能是控制毒砂中晶格金形成的主要因素。 相似文献
6.
美国内华达卡林金矿之含金FeS2微晶中不可见金的TEM研究和地球化学模型 总被引：1，自引：0，他引：1
透射电子显微术的研究表明,美国内华达州卡林金矿中环绕黄铁矿大 晶体的Fe的硫 化物微晶乃是白铁矿。该白铁矿含Au和As,并在其中有纳米尺度的似带状区。相对于邻区 而言,似带状区相对富As。因而提出：似带状区还相对富晶格金。根据所得出的方解石中三 价阳离子的分配系数方程认为,Au3＋阳离子是在白铁矿的非平衡(快速)结晶 作用期间,从白铁矿－溶液界面上被结合到细粒白铁矿中去的。Au3＋在白铁矿中的 配分是由非平衡分布系数(Kd')所控制的。然而,由于Au 3＋的平衡分 配系数(Kd)小,故通过平衡(缓慢)结晶作用形成的黄铁矿并不将Au 3 ＋结合到晶体中去。早期形成的细粒晶体的再结晶作用则将把REE和Au从晶体中迁移走。 相对于正常的白铁矿结构而言,较大的Au3＋和Au＋阳离子结合进入到白铁矿晶格 中,可引起局部的结构畸变,从而表现为似带状的特征。 相似文献
7.
利用原子力显微镜（AFM）、场发射高分辨率扫描电子显微镜（FESEM）和场发射高分辨率透射电子显微镜（HRTEM）对物理法改色前后的优质淡水珍珠表面进行了细致的观察。通过对比分析珍珠在微米级至纳米级的范围内微结构及超微结构特征的变化,证明珍珠质层是天然的纳米材料;改色前后珍珠的红外光谱分析及XRD分析对物理法改色珍珠机理是由于微量MnCO3在γ射线辐照下氧化成Mn2O3或MnO2所致的说法给予否定;由红外光谱测试结果可知物理法改色珍珠呈色机理与珍珠中有机物的辐照化学变化有关,并且物理法改色珍珠伴色的呈色机理与珍珠的文石纳米粒径效应亦无明显的相关性。 相似文献
8.
High resolution transmission electron microscopy evaluation of silica glaze reveals new textures 总被引：1，自引：0，他引：1
We present the first nanoscale investigation of silica glaze. High resolution transmission electron microscopy of a rock coating from the Ashikule Basin, Tibetan Plateau, reveals the presence of spheroids composed predominantly of silicon and oxygen with diameters ranging from 20 nm to 70 nm. While silica glaze spheroids co‐exist with manganese‐rich rock varnish in the same sample, the different rock coatings are texturally and physically distinct at the nanoscale. These observations are consistent with a model of silica glaze formation starting with soluble aluminum‐silicon (Al‐Si) complexes [Al(OSi(OH)3)2+], mobilized with gentle wetting events such as dew or frost. The transition between complete and partial wetting on silica surfaces rests at about 20–70 nm for liquid droplets. Upon crossing this transition, a metastable wetting film would be ruptured, initiating formation of silica glaze through spheroid deposition. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
9.
MENG Dawei WU Xiuling FAN Xiaoyu ZHANG Zhengjie CHEN Hong MENG Xin ZHENG Jianping 《《地质学报》英文版》2008,82(2):371-376
α-PbO2-type TiO2 （TiO2-Ⅱ） is an important index mineral for ultrahigh-pressure metamorphism. After the discovery of a natural high-pressure phase of titanium oxide with α-PbO2- structure in omphacite from coesite-bearing eclogite at Shima in the Dabie Mountains, China, a nanoscale （〈2 nm） α-PbO2-type TiO2 has been identified through electron diffraction and high-resolution transmission electron microscopy in coesite-bearing jadeite quartzite at Shuanghe in the Dabie Mountains. The crystal structure is orthorhombic with lattice parameters a = 4.58×10-1 nm, b = 5.42×10-1 nm, c = 4.96×10-1 nm and space group Pbcn. The analysis results reveal that ruffle {011}R twin interface is a basic structural unit of α-PbO2-type TiO2. Nucleation of α-PbO2-type TiO2 lamellae is caused by the displacement of one half of the titanium cations within the {011}R twin slab. This displacement reduces the Ti-O-Ti distance and is favored by high pressure. The identification of α- PbO2-type TiO2 in coesite-bearing jadeite quartzite from Shuanghe, Dabie Mountains, provides a new and powerful evidence of ultrahigh-pressure metamorphism at 4--7 GPa, 850℃-900℃, and implies a burial of continental crustal rocks to 130-200 kilometers depth or deeper. The α-PbO2-type TiO2 may be a useful indicator of the pressure and temperature in the diamond stability field. 相似文献
10.
珍珠显微结构及纳米矿物的电镜分析 总被引：2，自引：1，他引：1
采用SEM(扫描电子显微镜)和HRTEM(高分辨透射电子显微镜)技术,系统地研究了珍珠层及其微结构.发现珍珠质层是由有机质胶结的文石组成片状晶层,文石大量为六边形、不规则多边形和近圆形,并与有机质层交互平行叠置.在棱柱层的柱状晶体周围也有纤维状、胶状有机质.同时,在棱柱状和片状文石晶体的截面上,含有大量纳米级的圆形、椭圆形等形状的有机质、气液包裹体或孔洞.其中许多部位的有机基质中不同程度地显现出晶格条纹像,均为纳米矿物所致.以上结果均表明珍珠层具有有序、精细、多层次、整体性好等优良的结构特点.这一结论对于探讨珍珠的成因、机械强度及医药保健性能等方面均具有重要的意义. 相似文献