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1.
Dolomite [CaMg(CO3)2] forms in numerous geological settings, usually as a diagenetic replacement of limestone, and is an important component of petroleum reservoir rocks, rocks hosting base metal deposits and fresh water aquifers. Dolomite is a rhombohedral carbonate with a structure consisting of an ordered arrangement of alternating layers of Ca2+ and Mg2+ cations interspersed with anion layers normal to the c‐axis. Dolomite has symmetry, lower than the (CaCO3) symmetry of calcite primarily due to Ca–Mg ordering. High‐magnesium calcite also has symmetry and differs from dolomite in that Ca2+ and Mg2+ ions are not ordered. High‐magnesium calcite with near‐dolomite stoichiometry (≈50 mol% MgCO3) has been observed both in nature and in laboratory products and is referred to in the literature as protodolomite or very high‐magnesium calcite. Many dolomites display some degree of cation disorder (Ca2+ on Mg2+ sites and vice versa), which is detectable using transmission electron microscopy and X‐ray diffractometry. Laboratory syntheses at high temperature and pressure, as well as studies of natural dolomites show that factors affecting dolomite ordering, stoichiometry, nucleation and growth include temperature, alkalinity, pH, concentration of Mg and Ca, Mg to Ca ratio, fluid to rock ratio, mineralogy of the carbonate being replaced, and surface area available for nucleation. In spite of numerous attempts, dolomite has not been synthesized in the laboratory under near‐surface conditions. Examination of published X‐ray diffraction data demonstrates that assertions of dolomite synthesis in the laboratory under near‐ambient conditions by microbial mediation are unsubstantiated. These laboratory products show no evidence of cation ordering and appear to be very high‐magnesium calcite. Elevated‐temperature and elevated‐pressure experiments demonstrate that dolomite nucleation and growth always are preceded by very high‐magnesium calcite formation. It remains to be demonstrated whether microbial‐mediated growth of very high‐magnesium calcite in nature provides a precursor to dolomite nucleation and growth analogous to reaction paths in high‐temperature experiments.  相似文献   

2.
This paper presents a thermo‐hydro‐mechanical framework to model the drying behavior of Boom clay. First, the experimental campaign conducted Noémie Prime is briefly presented because it is used to validate the model. The data acquisition and processing is emphasized because of the use of X‐ray microtomography to be able to more accurately compare experimental and numerical strain fields. The different submodels are introduced. Numerical simulations are performed to illustrate the capability of the proposed model to reproduce the observed behavior. Finally, a comprehensive sensitivity study on several key model parameters associated with the water retention curve, and the permeability of the medium, is performed to get a better understanding of the physics behind the coupled model.  相似文献   

3.
There is an increasing use of analytical macro‐beam techniques (such as portable XRF, PXRF) for geochemical measurements, as a result of their convenience and relatively low cost per measurement. Reference materials (RMs) are essential for validation, and sometimes calibration, of beam measurements, just as they are for the traditional analytical techniques that use bulk powders. RMs are typically supplied with data sheets that tabulate uncertainties in the reference values by element, for which purpose they also specify a minimum recommended mass of material to be used in the chemical analysis. This minimum mass may not be achievable using analytical beam techniques. In this study, the mass of the test portion interrogated by a handheld PXRF within pellets made from three silicate RMs (SdAR L2, M2 and H1) was estimated using a theoretical approach. It was found to vary from 0.001 to 0.3 g for an 8 mm beam size and 0.0001 to 0.045 g for a 3 mm beam. These test portion masses are mainly well below the recommended minimum mass for these particular RMs (0.2 g), but were found to increase as a function of atomic number (as might be expected). The uncertainties caused by heterogeneity (UHET) in PXRF measurements of the three RMs were experimentally estimated using two different beam diameters for eighteen elements. The elements showing the highest levels of heterogeneity (UHET > 5%) seem generally to be those usually associated with either an accessory mineral (e.g., Zr in zircon, As in pyrite) or low test portion mass (associated with low atomic number). When the beam size was changed from nominally 8 to 3 mm, the uncertainty caused by heterogeneity was seen to increase for most elements by an average ratio of 2.2. These values of UHET were used to calculate revised uncertainties of the reference values that would be appropriate for measurements made using a PXRF with these beam sizes. The methods used here to estimate UHET in PXRF measurements have a potential application to other analytical beam techniques.  相似文献   

4.
Two‐phase fluid distributions in fractured porous media were studied using a single‐component multiphase (SCMP) lattice Boltzmann method (LBM), which was selected among three commonly used numerical approaches through a comparison against the available results of micro X‐ray computed tomography. The influence of the initial configuration and the periodic boundary conditions in the SCMP LBM for the fluid distribution analysis were investigated as well. It was revealed that regular porous media are sensitive to the initial distribution, whereas irregular porous media are insensitive. Moreover, to eliminate the influence of boundaries, the model's buffer size of an SCMP LBM simulation was suggested to be taken as approximately 12.5 times the average particle size. Then, the two‐phase fluid distribution of a porous medium was numerically studied using the SCMP LBM. Both detailed distribution patterns and macroscopic morphology parameters were reasonably well captured. Finally, the two‐phase fluid distributions in a fractured porous media were investigated. The influence of the degree of saturation, fracture length, and fracture width on the fluid distributions and migration was explored. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   

5.
X射线能谱仪测定宝石和玉石成分及磁化率测试   总被引：1，自引：0，他引：1  
刘刚  张子雄 《岩矿测试》1996,15(3):226-228
用Ｘ射线能谱仪对一些宝石、玉石样品进行了成分分析，并测试了磁化率。样品中含铁、铬氧化物者磁化率偏大，碧玺、玛瑙、合成刚玉及月光石的磁化率为负，表现出抗磁性  相似文献   

6.
Reaction and deformation microfabrics provide key information to understand the thermodynamic and kinetic controls of tectono‐metamorphic processes, however, they are usually analysed in two dimensions, omitting important information regarding the third spatial dimension. We applied synchrotron‐based X‐ray microtomography to document the evolution of a pristine olivine gabbro into a deformed omphacite–garnet eclogite in four dimensions, where the 4th dimension is represented by the degree of strain. In the investigated samples, which cover a strain gradient into a shear zone from the Western Gneiss Region (Norway), we focused on the spatial transformation of garnet coronas into elongated garnet clusters with increasing strain. The microtomographic data allowed quantification of garnet volume, shape and spatial arrangement evolution with increasing strain. The microtomographic observations were combined with light microscope and backscatter electron images as well as electron microprobe (EMPA) and electron backscatter diffraction (EBSD) analysis to correlate mineral composition and orientation data with the X‐ray absorption signal of the same mineral grains. With increasing deformation, the garnet volume almost triples. In the low‐strain domain, garnet grains form a well interconnected large garnet aggregate that develops throughout the entire sample. We also observed that garnet coronas in the gabbros never completely encapsulate olivine grains. In the most highly deformed eclogites, the oblate shapes of garnet clusters reflect a deformational origin of the microfabrics. We interpret the aligned garnet aggregates to direct synkinematic fluid flow, and consequently influence the transport of dissolved chemical components. EBSD analyses reveal that garnet shows a near‐random crystal preferred orientation that testifies no evidence for crystal plasticity. There is, however evidence for minor fracturing, neo‐nucleation and overgrowth. Microprobe chemical analysis revealed that garnet compositions progressively equilibrate to eclogite facies, becoming more almandine‐rich. We interpret these observations as pointing to a mechanical disintegration of the garnet coronas during strain localization, and their rearrangement into individual garnet clusters through a combination of garnet coalescence and overgrowth while the rock was deforming.  相似文献   

7.
Grain‐size distribution is a fundamental tool for interpreting sedimentary units within depositional systems. The techniques assessed in this study are commonly used to determine grain‐size distributions for sand‐dominated sediments. However, the degree of consistency and differences in interpretation when using a combination of grain‐size methods have not yet been assessed systematically for sand‐dominated fluvial sediments. Results obtained from laser diffraction, X‐ray attenuation and scanning electron microscopy grain‐size analysis techniques were compared with those obtained from the traditional sieve/hydrometer method. Scanning electron microscopy was shown to provide an inaccurate quantitative analysis of grain‐size distributions because of difficulties in obtaining representative samples for examination. The X‐ray attenuation method is unsuitable for sand‐dominated sediments because of its upper size range of only 300 μm. The consistently strong correlation between the laser diffraction results and the sieve/hydrometer results shows that these methods are comparable for sand‐dominated fluvial sediments. Provided that sample preparation is consistent, the latter two methods can be used together within a study of such sediments while maintaining a high degree of accuracy. These results indicate that data for sand‐dominated fluvial sediments gained from the long‐established sieve/hydrometer method can be compared with confidence to those obtained by modern studies using laser diffraction techniques.  相似文献   

8.
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9.
Quantitative X‐ray diffraction analysis of the <2 mm sediment fraction was carried out on 1257 samples (from the seafloor and 16 cores) from the Iceland shelf west of 18° W. All but one core (B997‐347PC) were from transects along troughs on the NW to N‐central shelf, an area that in modern and historic times has been affected by drift ice. The paper focuses on the non‐clay mineralogy of the sediments (excluding calcite and volcanic glass). Quartz and potassium feldspars occupy similar positions in an R‐mode principal component analysis, and oligoclase feldspar tracks quartz; these minerals are used as a proxy for ice‐rafted detritus (IRD). Accordingly, the sum of these largely foreign minerals (Q&K) (to Icelandic bedrock) is used as a proxy for drift ice. A stacked, equi‐spaced 100 a record is developed which shows both low‐frequency trends and higher‐frequency events. The detrended stacked record compares well with the flux of quartz (mg cm?2 a?1) at MD99‐2269 off N Iceland. The multi‐taper method indicated that there are three significant frequencies at the 95% confidence level with periods of ca. 2500, 445 and 304 a. Regime shift analysis pinpoints intervals when there was a statistically significant shift in the average Q&K weight %, and identifies four IRD‐rich events separated by intervals with lower inputs. There is some association between peaks of IRD input, less dense surface waters (from δ18O data on planktonic foraminifera) and intervals of moraine building. Copyright © 2009 John Wiley & Sons, Ltd.  相似文献   

10.
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11.
The sedimentological and geochemical properties of a 7·47 m long laminated sequence from hypersaline Lake Yoa in northern Chad have been investigated, representing a unique, continuous 6100 year long continental record of climate and environmental change in the eastern Central Sahara. These data were used to reconstruct the Mid to Late Holocene history of this currently hyper‐arid region, in order to address the question of whether the Mid Holocene environmental transition from a humid to a dry Sahara was progressive or abrupt. This study involved a suite of analyses, including petrographic and scanning electron microscope examination of thin sections, X‐ray diffraction, X‐radiography, granulometry, loss on ignition and magnetic susceptibility. The potential of micro‐X‐ray fluorescence core scanning was tested at very high resolution. Detailed microscopic investigation revealed the sedimentary processes responsible for the formation of the fine laminations, identified the season during which they were formed, and confirmed their annually rhythmic nature. High‐resolution X‐ray fluorescence core scanning allowed the distinction of each individual lamination over the entire record, opening new perspectives for the study of finely laminated sediment sequences. Geochemical and mineralogical data reveal that, due to decreasing monsoon rainfall combined with continuous and strong evaporation, the hydrologically open and fresh Mid Holocene Lake Yoa slowly evolved into the present‐day hypersaline brine depleted in calcium, which has existed for about the past 1050 years. During the oldest part of the investigated period, Lake Yoa probably contained a permanently stratified lower water column that was nevertheless disrupted relatively frequently by mixing events. Deep‐water anoxia became more stable because of increased salinity‐driven density stratification. In parallel, the sediment grain‐size proxies record a progressive increase of aeolian input in the course of the last 6100 years. Altogether, all geochemical and sedimentological indicators point to a progressive drying of the eastern Central Sahara, strengthening previous conclusions based on palaeoecological indicators.  相似文献   

12.
放射性同位素多道X荧光分析是一种核分析方法 ,具有快速、无损、低成本及多元素分析等优点。以华蓥山地区庙坝下三叠统嘉陵江组剖面为例 ,采用放射性同位素多道X荧光分析方法 ,测定了地层中Ca、Fe、Sr、Ba元素的照射率 ,并进行了化学地层和层序地层的初步研究 ,取得了较好的效果。  相似文献   

13.
The strong spectral interference between Br‐ and Al‐induced X‐ray lines hampers the utilisation of electron probe microanalysis (EPMA) for measuring Br mass fractions in Al‐bearing minerals and glasses. Through measuring Br‐free Al‐bearing materials, we established an EPMA method to quantify the overlap from AlKα on BrLβ, which can be expressed as a linear function of the Al2O3 content. The count rate of the BrLβ peak signal was enhanced by high beam currents and long measurement times. Application of this EPMA method to Al‐ and Br‐bearing materials, such as sodalite and scapolite, and to five experimental glasses yielded Br mass fractions (in the range of 250–4000 μg g?1) that are consistent with those measured by microbeam synchrotron X‐ray fluorescence (μ‐SXRF) spectrometry. The EPMA method has an estimated detection limit of ~ 100–300 μg g?1. We propose that this method is useful for measuring Br mass fractions (hundreds to thousands of μg g?1) in Al‐bearing minerals and glasses, including those produced in Br‐doped experiments. In addition, the natural marialitic scapolite (ON70) from Mpwapwa (Tanzania) containing homogeneously distributed high mass fractions of Br (2058 ± 56 μg g?1) and Cl (1.98 ± 0.03% m/m) is an ideal reference material for future in situ analyses.  相似文献   

14.
Although most of the world's uranium exists as pitchblende or uraninite, this mineral can be weathered to a great variety of secondary uranium minerals, most containing the uranyl cation. Anthropogenic uranium compounds can also react in the environment, leading to spatial–chemical alterations that could be useful for nuclear forensics analyses. Soft X‐ray absorption spectroscopy (XAS) has the advantages of being non‐destructive, element‐specific and sensitive to electronic and physical structure. The soft X‐ray probe can also be focused to a spot size on the order of tens of nanometres, providing chemical information with high spatial resolution. However, before XAS can be applied at high spatial resolution, it is necessary to find spectroscopic signatures for a variety of uranium compounds in the soft X‐ray spectral region. To that end, we collected the near edge X‐ray absorption fine structure (NEXAFS) spectra of a variety of common uranyl‐bearing minerals, including uranyl carbonates, oxyhydroxides, phosphates and silicates. We find that uranyl compounds can be distinguished by class (carbonate, oxyhydroxide, phosphate or silicate) based on their oxygen K‐edge absorption spectra. This work establishes a database of reference spectra for future spatially resolved analyses. We proceed to show scanning X‐ray transmission microscopy (STXM) data from a schoepite particle in the presence of an unknown contaminant.  相似文献   

15.
The paper is motivated by the long‐term safety analysis of the CO2 geological storage. We present a methodology for the assessment of the geomechanical impact of progressive rock dissolution. The method is based on the use of X‐ray tomography and the numerical dissolution technique. The influence of evolution of the microstructure on the macroscopic properties of the rock is analysed by using periodic homogenization method. The numerical computations show progressive degradation of all components of the stiffness (orthotropic) tensor. Moreover, the evolution of associated mass transfer properties (as tortuosity and conductivity tensors), by using the periodic homogenization method, is also calculated. The correlation between the mechanical parameters and the transfer properties during the dissolution process is presented. The results show that the highest increase of the hydraulic conductivity (in direction Y) is not associated with the highest decrease of Young modulus in this direction. Moreover, the highest decrease of Young modulus (in the direction X) is not associated with percolation in this direction. Finally, an incremental law to calculate settlement, in case of a rock with evolving microstructure, is proposed. The solution of the macroscopic settlement problem under constant stress and drained conditions showed that the geomechanical effects of the rock dissolution are rather limited. Copyright © 2014 John Wiley & Sons, Ltd.  相似文献   

16.
X射线荧光光谱法测定钒的原子价平均值   总被引：2，自引：1，他引：1  
孙伟莹  谭秉和 《岩矿测试》1998,17(3):193-196
用Ｘ射线荧光光谱法测定了一系列钒的氧化物混合物中Ｖ的Ｋβ谱线的精细结构,研究了钒的氧化物中Ｋβ谱峰参数随混合物平均原子价变化的规律,并利用所作的定标曲线对一些实际样品,如钒渣、磁铁矿中钒的平均原子价进行了定量测定。  相似文献   

17.
我国各地膨润土的矿物学性质   总被引：24，自引：3，他引：24  
运用X射线衍射分析技术对我国不同产地膨润土的矿物学性质进行考察；利用K值法测蒙脱石含量。实验表明，各地膨润土具有蒙脱石的含量较高且均为二八面体的矿物学特点；可能由于所处的矿层或局部地球化学环境不同，使得相同矿床的不同颜色膨润土矿物的蒙脱石含量有所差异。  相似文献   

18.
邓赛文  刘钢等 《岩矿测试》2001,20(3):237-240
介绍了日本理学公司3080系列X射线荧光光谱仪出现的几种故障现象，。分析判断及处理方法等。  相似文献   

19.
楼蔓藤 《岩矿测试》2002,21(1):42-48
简述了X射线荧光光谱分析方法标准化的进展，包括其意义与历史回顾、标准现状、不足与建议。主要参考文献33篇。  相似文献   

20.
遂安石是一种硼酸盐矿物 ,它的晶系归属一直是争论的问题。通过对辽吉硼矿床的遂安石的双晶观察、X射线衍射分析和电子衍射分析 ,结果表明它应是三斜晶系 ,β=10 4 .5°。  相似文献   

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