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1.
The morphological characteristics of the Zhongxiang (钟祥) rectorite have been studied using X-ray diffraction (XRD), electron probe micro-analyzer (EPMA), scanning electron microscopy (SEM), atomic force microscope (AFM), and high-resolution transmission electron microscopy (HRTEM). The structural formula of the Zhongxiang rectorite is: interstratification of (K, Na)-mica and Ca-montmorillouite. SEM observations show that Zhongxiang rectorite occurs as platy and fold-shaped crystals, and mainly as extremely thin plates with thickness ranging from 0.4 to 0.05 μm and a smooth (001) surface. There are well-developed polygonal steps on the surfaces of some thick crystals, suggesting a layer-by-layer growth mechanism. AFM observations show a series of steps with a height of 2 nm on the platy particles, suggesting the stacking of 20 nm fundamental particles. Club-like or fiber-shaped halloysite is included in the platy crystals with their elongated dimension paralleling (001) of the platy crystals or crossing the (001) surface of the platy rectorite, indicating multi-stage crystallization and involvement of hydrothermal fluids. The Zhongxiang rectorite was generated by both layer-by-layer growth mechanism and dissolution and crystallization growth mechanism with multistages.  相似文献   

2.
 Romanian amber (rumanite) has been considered to be a separate species of fossil resin for more than a century. While earlier investigators held it to be very similar to succinite (Baltic amber), modern scholars have assigned it a distinctly different botanical origin. We have found that almost all of the constituents of the ether-soluble fractions of 13 specimens of authentic rumanite identified by gas chromatography–mass spectrometry have previously been reported in the soluble fraction of succinite, including succinic acid and its monoterpene esters. Additionally and significantly, the soluble fraction of rumanite contains a number defunctionalized compounds that do not preexist in succinite, but that are produced by pyrolysis of whole succinite or of its insoluble polymeric fraction. Simultaneous methylation pyrolysis–gas chromatography–mass spectrometry of the polymeric fraction of seven of the rumanite specimens yielded further copious amounts of dimethyl succinate, a number of diterpene resin acid methyl esters, and additional defunctionalized compounds known to be pyrolysis products of succinite. The evidence shows conclusively that the botanical origin of rumanite is not distinct from that of succinite. Rather, rumanite is a succinite that has suffered partial thermal degradation in the course of the folding of the Oligocene Kliwa sandstone formation in which it is most commonly found. Received: 30 December 1999 / Accepted: 16 May 2000  相似文献   

3.
 The growth of K-jarosite was evaluated using scanning electron microscopy (SEM), atomic force microscopy (AFM), and molecular simulations. SEM micrographs show crystals with almost quadratic and, to a minor extent, triangular faces. These were identified to be {0 1 2} and (0 0 1) faces, respectively, using an X-ray single-crystal diffractometer. These results are in agreement with molecular simulations that show that the dipole-free {0 1 2} face is the most stable surface, followed by the (0 0 1) surface, that can lower its dipole moment perpendicular to the surface during relaxation. On the {0 1 2} face, the most stable step directions were identified. From these, an idealized equilibrium growth island can be constructed when the corner energies are minimized by the successive removal of corner ions until a stoichiometric growth island is obtained. Such an equilibrium growth island is the basis for developing a spiral growth model that explains the mechanism of spiral formation as observed using AFM. Furthermore, reactive sites that are potential candidates for the incorporation of foreign ions can be located. Received: 2 January 2001 / Accepted: 30 April 2001  相似文献   

4.
Glauconitic peloids from a Hauterivian condensed level in a hemipelagic unit of the Internal Prebetic (Los Villares Formation, eastern Betic Cordillera) have been studied by X‐ray diffraction (XRD), optical microscopy, scanning electron microscopy (SEM) and high‐resolution transmission electron microscopy (HRTEM) and analytical electron microscopy (AEM). The sediments forming the condensed level are characterized by abundant spherical to ovoid green glauconite peloids with radial cracks. Quartz, feldspar and muscovite are also abundant, whereas calcium phosphate is rarely detected. XRD analysis of the peloids reveals glauconite and small amounts of berthierine. SEM and HRTEM data show feldspar dissolution features, a Si–Al‐rich gel‐like substance filling K‐feldspar micropores and interlayering of well‐crystallized glauconite and berthierine packets. The last stage of the glauconitization process resulted in conversion of the smectitic precursor. Sedimentary and mineralogical features indicate an autochthonous origin for the glauconite. The depositional environment was a distal, hemipelagic ramp on the Southern Iberian Continental Palaeomargin. Low sedimentation rates lead to sediment condensation in a general transgressive context. The margin was affected by extensional tectonics, creating tilted blocks, resulting in lateral facies changes. The dissolution of K‐feldspars probably occurred after their deposition in the marine environment but predating the glauconitization. An influx of meteoric water is therefore required, probably related to subsurface fluxes from adjacent emergent areas (the higher parts of tilted blocks). Copyright © 2007 John Wiley & Sons, Ltd.  相似文献   

5.
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   

6.
本文叙述了贵州大方伊/蒙不规则间层粘土（I/S）的矿物学特征，包括矿物组成、化学成分、谱学特征、显微形貌特征以及理化特征，并对其应用前景进行了探讨。结合XRD和HRTEM两方面证据，获得了关于该矿物在C轴方向上的堆垛方式，三种以上共存的间层作用类型有力地证实了其不规则性。  相似文献   

7.
An exploratory study has been conducted to test the utility of automated mineral analysis observations to identify flue dust particles in topsoils exposed for several decades to emissions of a copper smelter. The methods used are readily available in mining countries. To identify the most impacted sites, the Cu, Zn, Pb, Mo and As levels in water and diluted sulphuric acid extractions of four topsoil size fractions (833–495 μm, 246–148 μm; 74–38 μm; <38 μm) were analysed. X-ray diffraction analyses were used to demonstrate the mineralogical degradation of smectite phases when approaching the smelter. Flue dust particles in different states of conservation in topsoils were directly observed by scanning electron microscopy (SEM) aided by energy dispersive detection of X-rays. Qemscan® scanning of dispersed topsoil preparations (10,000 particles) pinpoints smelter particles by their density; flue dust pearls can be tracked by sorting particles according to their sphericity, clearly identifying them as pyrometallurgical products. When sorting soil particles by mineral groups (e.g. sulphides), an increase in this phase group can be observed when approaching the smelter. SEM resolution limits observations to particles larger than 2–3 μm. Smaller particles can be observed by transmission electron microscopy, although observer experience and the availability of equipment time are essential as is the case for SEM.  相似文献   

8.
Ectomycorrhiza-forming fungi (EMF) alter the nutrient-acquisition capabilities of vascular plants, and may play an important role in mineral weathering and the partitioning of products of weathering in soils under nutrient-limited conditions. In this study, we isolated the weathering function of Suillus tomentosus in liquid-cultures with biotite micas incubated at room temperature. We hypothesized that the fungus would accelerate weathering by hyphal attachment to biotite surfaces and transmission of nutrient cations via direct exchange into the fungal biomass. We combined a mass-balance approach with scanning electron microscopy (SEM) and atomic force microscopy (AFM) to estimate weathering rates and study dissolution features on biotite surfaces. Weathering of biotite flakes was about 2-3 orders of magnitude faster in shaken liquid-cultures with fungus compared to shaken controls without fungus, but with added inorganic acids. Adding fungus in nonshaken cultures caused a higher dissolution rate than in inorganic pH controls without fungus, but it was not significantly faster than organic pH controls without fungus. The K+, Mg2+ and Fe2+ from biotite were preferentially partitioned into fungal biomass in the shaken cultures, while in the nonshaken cultures, K+ and Mg2+ was lost from biomass and Fe2+ bioaccumulated much less. Fungal hyphae attached to biotite surfaces, but no significant surface changes were detected by SEM. When cultures were shaken, the AFM images of basal planes appeared to be rougher and had abundant dissolution channels, but such channel development was minor in nonshaken conditions. Even under shaken conditions the channels only accounted for only 1/100 of the total dissolution rate of 2.7 × 10−10 mol of biotite m−2 s−1. The results suggest that fungal weathering predominantly occurred not by attachment and direct transfer of nutrients via hyphae, but because of the acidification of the bulk liquid by organic acids, fungal respiration (CO2), and complexation of cations which accelerated dissolution of biotite. Results further suggest that both carbohydrate source (abundant here) and a host with which nutrients are exchanged (missing here) may be required for EMF to exert an important weathering effect in soils. Unsaturated conditions and physical dispersal of nutrient-rich minerals in soils may also confer a benefit for hyphal growth and attachment, and promote the attachment-mediated weathering which has been observed elsewhere on soil mineral surfaces.  相似文献   

9.
The structures of prismatic (100) and pyramidal (101) growth faces of natural quartz crystals, and their modification upon annealing at T ≤ 400°C were investigated ex situ by atomic force microscopy (AFM) and in water by high-resolution X-ray reflectivity. AFM images revealed the presence of ∼ 0.1 to 1 μm-wide flat terraces delimited by steps of one to several unit cells in height. These steps follow approximately directions given by the intersection of growth faces. Modeling of X-ray reflectivity data indicates that surface silica groups on flat terraces have only one free Si-O bond each (presumably hydroxylated), except for some having two free Si-O bonds observed on a single (100) surface. Vertical relaxation of atomic positions (< 0.4 Å for terminal oxygens and < 0.2 Å for silicon and oxygen atoms fully coordinated to structural tetrahedra) is limited to a depth of 14 Å. Electron density profiles for all measured interfaces are consistent with a single layer of adsorbed water, with no evidence for additional organization of water molecules into distinct layers extending into the bulk solution. Similar interfacial structures were observed for natural and annealed surfaces of identical crystallographic orientation, indicating that extensive reconstruction of the silica network at the quartz surface did not occur under the annealing conditions.  相似文献   

10.
Atomic force microscopy (AFM) and Derjaguin-Landau-Verwey-Overbeek (DLVO) theory in combination with the interaction force boundary layer (IFBL) model have been used to empirically and theoretically calculate sticking efficiencies (α) of Enterococcus faecalis cells against a silica glass surface. Sticking efficiencies were calculated in solutions of varying pH and ionic strength and related to maximum distances of transport through a hypothetical soil block using colloid filtration theory.AFM measurements show that the repulsive and attractive forces between E. faecalis cells and a glass surface are a function of ionic strength but are less sensitive to changes in solution pH. Zeta (ζ)-potential measurements of the cells and glass surfaces correlate with these trends. Calculated DLVO energy profiles predict much greater sensitivity to changing solution chemistry. Sticking efficiencies derived from AFM measurements range from 9.6 × 10−17 to 1 in solutions of low ionic strength (IS) and from 2.6 × 10−33 to 1 at higher IS. Corresponding α values determined from DLVO theory are essentially zero in all tested solutions.Sticking efficiencies calculated in this study are smaller than values determined from column and field studies in similar systems; however, α derived from AFM data and the IFBL model more closely represent field data than do values calculated from DLVO energy values. A comparison with different methods of calculating α suggests that reversible adhesion may be significant in column-scale transport studies.  相似文献   

11.
Magnesite (104) dissolution kinetics were studied in acidic aqueous solutions (2.0 < pH < 4.2) at temperatures between 60 and 90°C by atomic force microscopy (AFM). Comparison of dissolution fluxes obtained by AFM and chemical methods revealed six to seven times larger dissolution fluxes obtained by chemical analysis. Corresponding empirical activation energies were found to be 74 ±22 kJ/mol and 41 ± 4 kJ/mol (at pH 4.2) for the AFM and chemical methods, respectively. The empirical reaction order with respect to proton concentration was 0.36 ± 0.13 and 0.47 ± 0.03 for AFM and chemical methods, respectively. These comparisons suggest that the two experimental measurement methods differ as a result of the different sampling length scales associated with the methods. Negligible changes in step dissolution velocity with changes in bulk pH were found, suggesting that the principal source of increasing dissolution flux with decreasing pH is an increase in step density. However, the observed stable step orientation, which is dependent on pH, suggests that more than one proton adsorption equilibrium should be used to describe the surface chemistry of magnesite in acidic solution.  相似文献   

12.
Magnesium inhibition of calcite dissolution kinetics   总被引：1，自引：0，他引：1  
We present evidence of inhibition of calcite dissolution by dissolved magnesium through direct observations of the (104) surface using atomic force microscopy (AFM) and vertical scanning interferometry (VSI). Far from equilibrium, the pattern of magnesium inhibition is dependent on solution composition and specific to surface step geometry. In CO2-free solutions (pH 8.8), dissolved magnesium brings about little inhibition even at concentrations of 0.8 × 10−3 molal. At the same pH, magnesium concentrations of less than 0.05 × 10−3 molal in carbonate-buffered solutions generate significant inhibition, although no changes in surface and etch pit morphology are observed. As concentrations exceed magnesite saturation, the dissolution rate shows little additional decrease; however, selective pinning of step edges results in unique etch pit profiles, seen in both AFM and VSI datasets. Despite the decreases in step velocity, magnesium addition in carbonated solutions also appears to activate the surface by increasing the nucleation rate of new defects. These relationships suggest that the modest depression of the bulk rate measured by VSI reflects a balance between competing reaction mechanisms that simultaneously depress the rate through selective inhibition of step movement, but also enhance reactivity on terraces by lowering the energy barrier to new etch pit formation.  相似文献   

13.
The defect structure of zeolite (K+, TMA+) — ZK-14, a synthetic chabazite, has been studied using scanning electron microscopy (SEM) and transmission electron microscopy (TEM). SEM together with TEM bright field (BF) and dark field (DF) micrographs indicate that the hexagonal, platelet ZK-14 crystals are built up of crystalline blocks joined by twinning along (00.1). High resolution transmission electron microscopy (HRTEM) reveals faulting of the ideal AABBCC single 6-ring stacking sequence of ZK-14. This is consistent with an observed line broadening in its X-ray powder diffraction profile. Channel apertures are imaged, even for thick specimens.  相似文献   

14.
Series of sedimentary hydrothermal-diplogenetic copper deposits have been found scattering in the region along the middle-lower reaches of the Yangtze River, and their metallogenetic mechanism is still in hot debate. In order to reveal the ore-forming kinetics of sedimentary process and hydrothermal superimposition, and evaluate the role of sedimentary pyrite in the enrichment and precipitation of copper, a set of simulating experiments on the reaction between pyrite and CuCl2 solution were conducted. According to the physicochemical characteristics of the ore-forming fluid of the Dongguashan copper deposit, Anhui Province, 100 MPa was selected as the experimental pressure, and the experimental temperatures were set at 450, 350, 250 and 150°C, respectively. The reactions between pyrite grains isolated from the Shimenkou strata-bound pyrite deposit and the solution with 0.2 mol/L CuCl2 and 1.0 mol/L NaCl were experimentally simulated. Then, variations in surface topography and surface chemistry of the experimental pyrite grains were documented using scanning electronic microscopy (SEM), atomic force microscopy (AFM), Auger electron spectrometry (AES) and X-ray photoelectron spectroscopy (XPS), and the solution and newly formed minerals were analyzed using inductively coupled plasma (ICP-AES) and X-ray diffraction (XRD) techniques. Desulphurization of pyrite surface was observed and new copper minerals were detected. It is proposed that pyrite can act as a geochemical barrier for the enrichment and precipitation of copper from the solution under the experimental conditions. Furthermore, the ore-forming mechanism of sedimentary hydrothermal-diplogenetic copper deposits was discussed.  相似文献   

15.
In situ atomic force microscopy (AFM) was used to study the molecular-scale reactivity of anhydrite (1 0 0), (0 1 0), and (0 0 1) faces exposed to water and CaSO4 aqueous solutions at room temperature. In pure water, dissolution occurs by step retreat and etch pit nucleation and growth. Both the kinetics of the step retreat and the shape of the etch pits are surface-specific and crystallographically controlled. In CaSO4 aqueous solutions with concentrations ranging from 0.030 mol/l to 0.075 mol/l, the growth kinetics on anhydrite (1 0 0) and (0 1 0) faces was studied. Growth is also strongly controlled by crystallographic constraints and occurs exclusively from pre-existing step edges by highly anisotropic spreading of monolayers (3.5 Å in height). The AFM observations demonstrate that monolayer growth can occur on anhydrite (0 1 0) and (1 0 0) faces even from slightly supersaturated solutions. In addition, the comparison of the step kinetics on anhydrite faces shows that the mechanisms of step dissolution and growth are essentially the same, with the direction of migration of crystal building units being reversed at the anhydrite saturation point. Moreover, the analysis of both high resolution AFM images and lateral force microscopy (LFM) images confirms that the newly-formed monolayers are anhydrite growing in structural continuity with the original (1 0 0) and (0 1 0) surfaces. However, the formation of the first monolayers is metastable and two-dimensional nucleation and further multilayer growth of anhydrite are strongly inhibited even at high supersaturations.  相似文献   

16.
We have examined microstructures, mineralogical composition, geochemical alteration, and texture of four selected fault rock samples from the Deep Geodynamical Laboratory (DGLab) Gulf of Corinth project using optical microscopy, cathodoluminescence microscopy (CL), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and synchrotron X-ray diffraction measurements. The fault core is composed of red and gray clayey gouge material and surrounded by a damage zone of brecciated limestones. Pressure solution features, calcite veins and calcite clasts in the breccia and gouge material attest the presence of paleo-fluids and fluid-driven mass transfer during deformation. Differences in CL-colors between the matrix and calcite vein cement and inside the vein cement suggest repeated infiltration of fluids with different composition from various sources (formation water and meteoric water). Twin lamellae densities estimated in calcite veins are used as paleo-piezometer. The deduced differential stress is ∼140 ± 70 MPa for the older vein generation and appears to be higher than stress for the youngest veins (45 ± 23 MPa). In spite of the relatively small clay content in both samples, newly formed clay minerals have been observed in gray as well as red clayey gouge material. Differences between gray and red clay gouge material are found in fault rock composition, porosity and clay fabric. The proportion of chlorite in the red gouge is significantly less than that in the gray gouge whereas the initial porosity is significantly higher than in the gray gouge material. The detection of a well-oriented clay fabric in red clay gouge samples is unique in comparison to other major fault zones.  相似文献   

17.
The micro- and nanostructures of modern and fossil aragonitic nacreous layers of cephalopod shells were studied with scanning electron microscope (SEM) and atomic force microscope (AFM). The nacreous tablets are organized in sectors, composed of acicular units. The acicular units are composed of small granules. The fossil and modern shells show some differences in granule size, but the granules are surrounded by a thin envelope in both samples. Electrophoretic and amino-acid compositions show that organic matrices are present in the fossil shells. Thus, the organic nature of the granule envelopes can be inferred from the two analytical approaches. The AFM microscopy allows us to study the nanostructures of the recent and fossil hard tissues and to observe the diagenetic changes of both the mineral and organic components.  相似文献   

18.
利用场发射高分辨率扫描电子显微镜（FESEM）、原子力显微镜（AFM）和场发射高分辨率透射电子显微镜（HRTEM）对广西合浦所产的具伴色和不具伴色的优质白色海水珍珠表面进行了系统的观察。通过对比分析珍珠在微米级至纳米级范围内微结构及超微结构特征的变化,证明了珍珠质层是天然的纳米材料,组成文石晶层的3μm文石小晶片是由10～60 nm的纳米文石小晶粒组成,珍珠伴色与其表面生长机理纹规则与否相关。  相似文献   

19.
 Characteristic samples of Upper Cretaceous pelagic red sediments from different parts of the Eastern Pontides (NE Turkey) have been investigated by X-ray diffraction (XRD), X-ray fluorescence (XRF) and scanning electron microscopy coupled with energy dispersive analyses (SEM/EDAX). The red sediments are composed of limestone and muddy limestone, and characterized by abundant planktonic foraminifers. Hematite content ranges from 0.5 to 3.0 wt.%. Electron microscope observations suggest that the hematite pigment has a diagenetic origin. The red colour is due to presence of hematite pigment, and indicates oxidizing conditions during early diagenesis in a relatively deep marine environment. Received: 4 January 1999 / Accepted: 8 July 1999  相似文献   

20.
The present study deals with the direct determination of colloidal forms of iron in river-borne solids from main rivers of the Amazon Basin. The contribution of different forms of colloidal iron have been assessed using ultrafiltration associated with various techniques including electron paramagnetic resonance spectroscopy (EPR), high resolution transmission electron microscopy (HRTEM), and micro proton-induced X ray emission analysis (μPIXE). EPR shows the presence of Fe3+ bound to organic matter (Fe3+-OM) and colloidal iron oxides. Quantitative estimate of Fe3+-OM content in colloidal matter ranges from 0.1 to 1.6 weight % of dried solids and decreases as the pH of the river increases in the range 4 to 6.8. The modeling of the field data with the Equilibrium Calculation of Speciation and Transport (ECOSAT) code demonstrates that this trend is indicative of a geochemical control resulting from the solubility equilibrium of Fe oxyhydroxide phase and Fe binding to organic matter. Combining EPR and μPIXE data quantitatively confirms the presence of colloidal iron phase (min. 35 to 65% of iron content), assuming no divalent Fe is present. In the Rio Negro, HRTEM specifies the nature of colloidal iron phase mainly as ferrihydrite particles of circa 20 to 50 Å associated with organic matter. The geochemical forms of colloidal iron differentiate the pedoclimatic regions drained by the different rivers, corresponding to different major weathering/erosion processes. Modeling allows the calculation of the speciation of iron as mineral, organic and dissolved phases in the studied rivers.  相似文献   

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