共查询到20条相似文献，搜索用时 46 毫秒
1.
J.C. Crelling I.J. Glasspool J.R. Gibbins M. Seitz 《International Journal of Coal Geology》2005,64(3-4):204-216
Although bireflectance measurements are routine, to date they have been limited to selected single point measurements. This study uses a 360° rotating polarizer in the incident light path combined with digital imaging to map the optical bireflectance of a polished specimen over the complete field of view, a system herein referred to as ‘Bireflectance Imaging of Coal and Carbon Specimens’ (BRICCS). True maximum reflectance maps and maps of polarizer angle for maximum reflectance (to identify co-ordered regions) are obtainable from the same data. A variety of coal, coke, char, graphite, and carbon/carbon specimens have been examined with the BRICCS system and the results demonstrate that the system can produce accurate maximum and apparent minimum reflectance, bireflectance, and extinction angle images. For example, flakes of natural graphite show no bireflectance along their long axis except in areas that have been strained. The images are maps showing the value of every pixel that has been calibrated by mineral reflectance standards. The maps are unique in that they show fields of view that cannot be seen by normal viewing through the microscope. For example, the bireflectance maps show the maximum difference between the maximum and apparent minimum reflectances for each of the million pixels at twenty orientations of the polarizer. 相似文献
2.
沉积物中有机质及相关元素含量、重金属含量等是研究环境污染和古环境的依据。利用近红外漫反射光谱测定沉积物中的化学成分,方法简便、快捷、价廉。本文概述了近红外漫反射光谱测定沉积物中化学成分的基本流程、样品制备及建模方法,介绍了如何通过选择建模样品、利用光谱预处理及回归分析等方法提高近红外光谱模型的定量能力,综述了近红外漫反射光谱分析沉积物中的有机碳、总氮、总磷、生物硅、重金属含量等方法。但是利用近红外光谱分析沉积物中的化学成分研究起步较晚,仍存在很多问题,有必要深入探讨近红外光谱分析沉积物的化学成分时产生误差的机理,进一步开展建模样品的计算机选择方法、光谱预处理方法和数学模型优化等方面的研究,提高近红外漫反射光谱分析沉积物中化学成分的精密度和准确度。 相似文献
3.
Abstract. Near-infrared (NIR) and visible light microthermometry was applied to the fluid inclusions in sphalerite from a possible southeast extension of the Toyoha polymetallic deposit. Sphalerite occurs as euhedral-subhedral crystals or collo-form aggregates with a variety of color, which contain a well-developed growth banding. Combined with morphological observations, fluid inclusions in dark-colored sphalerite were examined using a near-infrared light microscopic technique, whereas those in light-colored sphalerite and quartz were examined by a conventional visible light microscopy.
Salinities of fluid inclusions in dark-colored sphalerite have a wide variation (1.0–10.3 wt % NaCl equiv.) compared to that in light-colored sphalerite and quartz (0.0–3.4 wt % NaCl equiv.). These variations suggest that the conventional microthermometric data from light-colored sphalerite and quartz were inadequate to interpret the ore formation process. Dark-colored colloform sphalerite and a dark core of subhedral sphalerite formed from high-salinity fluids (6.5–10.3 wt % NaCl equiv.) under highly supersaturated conditions with respect to sphalerite.
The NIR and visible light microthermometry of fluid inclusions in sphalerite combined with its morphological observations is an invaluable method to infer the formation conditions of sphalerite. The NIR and visible light microthermometry is useful to reveal how the nature of ore fluids changed with time. 相似文献
Salinities of fluid inclusions in dark-colored sphalerite have a wide variation (1.0–10.3 wt % NaCl equiv.) compared to that in light-colored sphalerite and quartz (0.0–3.4 wt % NaCl equiv.). These variations suggest that the conventional microthermometric data from light-colored sphalerite and quartz were inadequate to interpret the ore formation process. Dark-colored colloform sphalerite and a dark core of subhedral sphalerite formed from high-salinity fluids (6.5–10.3 wt % NaCl equiv.) under highly supersaturated conditions with respect to sphalerite.
The NIR and visible light microthermometry of fluid inclusions in sphalerite combined with its morphological observations is an invaluable method to infer the formation conditions of sphalerite. The NIR and visible light microthermometry is useful to reveal how the nature of ore fluids changed with time. 相似文献
4.
Mina Moradizadeh Mehdi Momeni Mohammad R. Saradjian 《Arabian Journal of Geosciences》2014,7(5):1891-1897
Atmospheric water vapor validation needs simultaneous, well-defined, and independent information which are not easily available causing limitations in the development of remote sensing water vapor retrieval algorithms. This study is concerned with the retrieval of total atmospheric water vapor content and its validation. A band ratio method has been used to estimate the water vapor content based on Moderate Resolution Imaging Spectroradiometer (MODIS) Near InfraRed (NIR) data. The method uses MODIS bands 17, 18, and 19 as NIR bands and band 2 to remove the land cover reflectance. Furthermore, the Atmospheric Infrared Sounder (AIRS) has been used for both algorithm development and analysis of the results. The method has been modified to take into account the dry condition of the central parts of Iran. Using some various datasets, the method is implemented and evaluated quantitatively. The validation of the water vapor estimates has been undertaken by an analysis of AIRS data. The validation results shows error as low as 9 % for the estimated water vapor using the MODIS NIR band ratio method. 相似文献
5.
An infrared routine has been developed to estimate the aliphatic portion of kerogen carbon in sedimentary rocks. The procedure does not require isolation of the organic matter and is based on a computer-assisted determination of global band areas in the region of the aliphatic carbon-hydrogen stretching vibrations around 2900cm−1. From these integrated absorptions the amount of aliphatic carbon Cal (mg of aliphatic carbon per gram of solvent-extracted rock) is calculated by means of a calibration with model rocks. Carbonate overtones which interfere in the case of limestones are eliminated by comparison to a CaCO3 standard.The method has been applied to rocks containing kerogens of different types and maturities at TOC levels of 0.5 to 12%. The aliphatic carbon concentrations range from 0.5 to 60mg·g−1 and correlate reasonably well with the residual genetic potentials of the rocks as measured by S2 values from Rock-Eval pyrolysis. The ratio S2/Cal is found to decrease with burial depth reflecting a maturity enhanced conversion of aliphatic carbon to fixed aromatic carbon under Rock-Eval conditions. 相似文献
6.
利用偏最小二乘法回归的多变量校正方式,建立了应用近红外反射光谱学方法无损快速测定各种地质样品中有机质的模型.设计了多重散射光校正、标准正常变量转换及导数光谱,扣除额外基线和重叠信号的影响,分离出与有机质含量有关的光谱信息.大多数地质样品的有机质近红外反射光谱估算结果与化学法符合. 相似文献
7.
对采自青藏高原北部渐新统雅西措组中的叠层石样品进行了研究,通过切面观察和薄片鉴定,确定这些叠层石具有典型的富藻生物纹层和富屑碎屑纹层交替的显微结构特征,纹层生长带呈阶段式波状和柱状产出。采用样品数字图像的灰度值作为计量纹层个数和纹层厚度变化的指标,提取了4件样品的显微纹层厚度变化序列。根据功率谱分析结果,认为叠层石纹层层偶为年际生长纹层,纹层层偶的厚度变化与太阳黑子活动的11年天文周期具有一定的联系,提出湖相环境中叠层石的生长节律记录了太阳活动驱动的气候与环境变化的信息。 相似文献
8.
衡阳市郊五马归槽始新世鱼化石保存在黑色湖相纹层中。根据纹层序列的对比,发现该地的鱼化石均为同一层位;根据鱼化石在纹层序列中的具体位置及鱼化石的保存状况,笔者推测鱼群的死亡并非由于季节更替,而是由气候干旱引起的湖水盐度升高所控制;黑白纹层的变化是由大气降雨所致。 相似文献
9.
A critical evaluation has been made of the thermodynamic properties reported in the literature for 43 organic iodine compounds in the solid, liquid, or ideal gas state. These compounds include aliphatic, cyclic and aromatic iodides, iodophenols, iodocarboxylic acids, and acetyl and benzoyl iodides. The evaluation has been made on the basis of carbon number systematics and group additivity relations, which also allowed to provide estimates of the thermodynamic properties of those compounds for which no experimental data were available. Standard molal thermodynamic properties at 25 °C and 1 bar and heat capacity coefficients are reported for 13 crystalline, 29 liquid, and 39 ideal gas organic iodine compounds, which can be used to calculate the corresponding properties as a function of temperature and pressure. Values derived for the standard molal Gibbs energy of formation at 25 °C and 1 bar of these crystalline, liquid, and ideal gas organic iodine compounds have subsequently been combined with either solubility measurements or gas/water partition coefficients to obtain values for the standard partial molal Gibbs energies of formation at 25 °C and 1 bar of 32 aqueous organic iodine compounds. The thermodynamic properties of organic iodine compounds calculated in the present study can be used together with those for aqueous inorganic iodine species to predict the organic/inorganic speciation of iodine in marine sediments and petroleum systems, or in the near- and far-field of nuclear waste repositories. 相似文献
10.
Covalent and non-covalent interaction of proteinaceous materials in soils and sediments has been suggested as an important mechanism for immobilizing nitrogen in numerous types of environments. In a previous study (Hsu P.-H., Hatcher, P.G., 2005. New evidence for covalent coupling of peptides to humic acids based on 2D NMR spectroscopy: A means for preservation. Geochimica et Cosmochimica Acta 69, 4521–4533), we provided molecular evidence for covalent, as well as non-covalent, bonding between 15N-labeled peptides and humic acid molecules using the 2D HSQC (heteronuclear single quantum coherence) NMR technique. In this report, we examine the influence of aromaticity and aliphaticity of peptides and humic materials on these covalent and non-covalent interactions. We use 2D NMR techniques to evaluate bonding interactions of 15N labeled peptides, having different aromatic and aliphatic properties, with three humic acids that vary in degree of aromaticity. The peptide containing primarily aromatic amino acid residues is observed to form covalent and non-covalent bonds with mainly aromatic-rich humic acids. The peptide composed of aliphatic amino acid residues shows, on the other hand, only bonding interactions with aliphatic-rich humic acids. These observations provide the first direct molecular evidence that aliphatic functional groups are involved in bonding with proteinaceous materials. The process may play an important role in sequestration of proteinaceous materials in sedimentary systems such as marine systems where the humic materials are mainly aliphatic in nature. 相似文献
11.
B. Ramesh Babu B.E. P.G.D.C.A. Ph.D. S. Maruthamuthu M.Sc. M.Phil. Ph.D. A. Rajasekar M.Sc. N. Muthukumar M.Sc. M.Phil. N. Palaniswamy M.Sc. Ph.D. 《International Journal of Environmental Science and Technology》2006,3(2):159-166
In the dairy industry mild steel is used as the construction material for the effluent treatment plants, pipelines, reinforcement in concrete structures etc. The steel exposed to the dairy effluent faces corrosion due to the microbes. In the present study the role of microbes in dairy effluent on the corrosion of mild steel has been investigated. Pseudomonas sp., Streptococcus sp., Micrococcus sp., Bacillus sp., Neisseria sp. and Lactobacillus sp. were identified in dairy effluent. Corrosion rate has been estimated by weight loss measurements and polarization technique. The Fourier transform infrared spectroscopy (FTIR) and X-ray diffractometer (XRD) studies were found helpful in investigating the chemical pathway leading to the formation of corrosion products on the mild steel during fermentation. Initiation of pitting corrosion was noticed on steel specimens by scanning electron microscope (SEM). A mechanism has been proposed for microbiologically influenced corrosion in dairy effluent. 相似文献
12.
孙玉壮 《中国地球化学学报》2000,19(1):65-84
A study of the influences of the basin brines on hydrocarbon generation of the Kupferschiefer in southwestern Poland has been carried out.The samples from the Konrad and Polkowics mines were analyzed by orgainc geochemical,microscopic and FTIR methods.The results indicate that organic matter of Kupferschiefer tends to decrease with the ascending,oxidizing brines,In the Konrad profile,the Kupferschiefer was strongly oxidized.The extract yields were depleted up to 50mg Ext/g Corg.Gas chromatography(GC) and gas chromatography-mass spctrometry(GC/MS) data indicate that the depletion occureed predominantly in saturated hydrocarbon compounds.The identified n-alkanes in smpale KD1 were depleted at least to 5000μg/g Corg.The aromatic compounds show a fidderent trend of variation.The concentrations of phenanthrene alkylphenanthrenes(Ph-PAH) and naphthalene alkylnaphthalenes(Na-PAH) show a decrease,whereas sulfur polyaromatic hydrocarbons(S-PAH)and oxygen polyaromatic hydrocarbons(O-PAH) show an incrase under the influences of oxidizing brines,In the Polkowice profile,organic matter under the influences of oxidizing fluids shows a simlar trend of varation as in the Konrad mine.Analyses of polar compounds shed light on the oxidation processes at the molecule level.The dominant products of oxidation are aliphatic acid.alcohol and ester.FTIR results indicate that the oxidation of organic matter led to a decrease in aliphatic CH3 and an increase in C-O,C=O bands. 相似文献
13.
《Quaternary Science Reviews》2003,22(10-13):1329-1334
In optically stimulated luminescence dating, apparent ages of individual grains are thought to reflect a wide distribution of initial bleaching levels in hard to bleach sediments. Although having a larger age range (up to 1 Ma and beyond), this approach has not been used yet in electron spin resonance (ESR) dating. Here we report on the first results of ESR measurements on single sedimentary quartz grains. Initial bleaching levels are evaluated for two different River Meuse deposits in Limburg, NE Belgium. Measurements were done with a Q-band ESR spectrometer on transparent quartz grains of sufficiently large diameter (0.5–0.7 mm). Single crystal ESR properties were used to identify different ESR active centres. In about 50% of the selected grains an Al and/or Ti–Li signal was detected and the latter has been selected for further measurements. Artificial bleaching experiments show a strong signal decrease with UV light exposure. After gamma-ray irradiation, a number of different signal intensity vs. artificial dose curves could be observed: exponential growth, exponential saturation, linear, with inflexion points, and unclear ones. Many grains show increasing ESR signals with doses up to 1000 Gy, suggesting that the age range could be extended over 1 Ma, covering the Middle Pleistocene and part of the Early Pleistocene. Accumulated doses of individual grains were calculated using the additive dose method. The results show a large dose distribution of individual grains for both deposits. It is concluded that insufficiently bleached grains can be detected using single grain ESR measurements of sedimentary quartz in a fluvial environment. 相似文献
14.
This work presents geochemical characterization of isolated kerogen out of clay fraction using petrography studies, infrared absorption and solid state 13C nuclear magnetic resonance (NMR) spectroscopy, with N‐alkane distributions of saturated hydrocarbon. Mineralogical study of clay mineral associations was carried out using X‐ray diffraction (XRD), on Ypresian phosphatic series from Gafsa‐Metlaoui basin, Tunisia. The XRD data indicate that smectite, palygorskite and sepiolite are the prevalent clay minerals in the selected samples. In this clay mineral association, the N‐alkane (m/z = 57) distribution indicates that the marine organic matter is plankton and bacterial in origin. The kerogens observed on transmitted light microscopy, however, appear to be totally amorphous organic matter, without any appearance of biological form. The orange gel‐like amorphous organic matter with distinct edges and homogenous texture is consistent with a high degree of aliphaticity. This material has relatively intense CH2 and CH3 infrared bands in 13C NMR peaks. This aliphatic character is related to bacterial origin. Brown amorphous organic matter with diffuse edges has a lower aliphatic character than the previous kerogen, deduced from relatively low CH2 and CH3 infrared and 13C NMR band intensities. 相似文献
15.
流体包裹体是古地质流体的唯一直接记录,为反演地质过程涉及的物理化学条件等提供了最为重要的证据。流体包裹体是研究热液矿床成矿流体最有利手段,常规的测试对象为透明的脉石矿物,而矿石矿物中的流体包裹体更为直接、准确地记录了成矿流体信息。大多数矿石矿物在显微镜透射光下不透明,其捕获的流体包裹体研究需要使用配备有红外成像系统的显微镜进行。近20 年来,不透明矿物流体包裹体红外显微测温研究获得了长足的进展,但其中仍有一些问题尚未解决,制约了该方法的应用;同时,国内该研究领域正处在起步阶段,多个实验室已安装了红外测试仪器,但尚未开展系统的研究工作。因此,需要对该研究领域进行综述,探讨存在的问题,以促进该研究方法的发展。本文首先介绍了红外显微镜仪器工作原理及样品制备注意事项,阐述了影响不透明矿物红外透明度的因素,讨论了红外显微测温研究中的主要问题和难点,并针对测温过程中相变观察困难、红外光可能影响测温结果等问题提出可行的解决方案,最后论述了红外显微测温系统在矿床学领域的应用前景。 相似文献
16.
最近NGTC实验室检测出多批次CVD合成钻石,这些CVD合成钻石均具有明显的鉴定特征,使用钻石观测仪（DiamondViewTM）观察可见蓝色、橙红色荧光和蓝色磷光以及细密层状生长纹理,光致发光光谱中可见737 nm处的特征发光线.这些特征均与其生长结构及生长过程中进入钻石晶体中的杂质有关.笔者以最近检测过程中发现的一颗CVD合成钻石为例,使用高倍率显微技术对其层状结构的微细特征及其在钻石观测仪下的荧光特征的关系进行了详细观察和对比.结果显示,此样品与之前检测到的CVD合成钻石略有差异.此次检测到的样品在钻石观测仪（DiamondViewTM）下观察具有较宽的层状生长分区,层与层之间的分界线十分明显且在高倍显微镜下也可见到细微的生长特征.通过对样品特征的分析,了解了晶体生长过程中多阶段生长条件的变化,更直观的展现了CVD合成钻石的生长过程. 相似文献
17.
Chemical structure of Jurassic vitrinites isolated from the coals in basins in NW China have been checked using solid state 13C NMR and flash pyrolysis-GC/MS. Study shows some Jurassic collodetrinites are rich in aliphatic products in pyrolysates, consisting with the high amount of methylene carbon in 13C NMR spectra. In contrast, pyrolysates of Jurassic collotelinites are rich in phenols and alkylbenzenes. Also one Pennsylvanian and one Permian vitrinite selected from the Ordos basin, NW China have been checked for comparison. The proportion of aliphatics is low in pyrolysates, and aliphatic carbon peak in 13C NMR spectrum of Permian vitrinite is mostly composed of gas-prone carbons compared with collodetrinites in those Jurassic basins. But both pyrolysis and 13C NMR data shows the Pennsylvanian vitrinite is not only gas-prone but also oil-prone. Relatively high proportion of long chain aliphatic structure of some Jurassic vitrinite in Junggar, Turpan-Hami basins may be due to the contribution of liptodetrinites, which may be included during the formation of vitrinites. And it seems that suberinite is the most possible precursor of long chain aliphatics in the structure of Jurassic collodetrinite. 相似文献
18.
19.
《地学前缘(英文版)》2016,7(6)
Banded iron formations(BIFs) are major rock units having hematite layers intermittent with silica rich layers and formed by sedimentary processes during late Archean to mid Proterozoic time. In terrestrial environment, hematite deposits are mainly found associated with banded iron formations. The BIFs in Lake Superior(Canada) and Carajas(Brazil) have been studied by planetary scientists to trace the evolution of hematite deposits on Mars. Hematite deposits are extensively identified in Meridiani region on Mars. Many hypotheses have been proposed to decipher the mechanism for the formation of these deposits. On the basis of geomorphological and mineralogical studies, aqueous environment of deposition is found to be the most supportive mechanism for its secondary iron rich deposits. In the present study, we examined the spectral characteristics of banded iron formations of Joda and Daitari located in Singhbhum craton in eastern India to check its potentiality as an analog to the aqueous/marine environment on Mars. The prominent banding feature of banded iron formations is in the range of few millimeters to few centimeters in thickness. Fe rich bands are darker(gray) in color compared to the light reddish jaspilitic chert bands. Thin quartz veins(4 mm) are occasionally observed in the handspecimens of banded iron formations. Spectral investigations have been conducted in VIS/NIR region of electromagnetic spectrum in the laboratory conditions. Optimum absorption bands identified include 0.65, 0.86, 1.4 and 1.9 mm, in which 0.56 and 0.86 mm absorption bands are due to ferric iron and 1.4 and1.9 mm bands are due to OH/H_2O. To validate the mineralogical results obtained from VIS/NIR spectral radiometry, laser Raman and Fourier transform infrared spectroscopic techniques were utilized and the results were found to be similar. Goethite-hematite association in banded iron formation in Singhbhum craton suggests dehydration activity, which has altered the primary iron oxide phases into the secondary iron oxide phases. The optimum bands identified for the minerals using various spectroscopic techniques can be used as reference for similar mineral deposits on any remote area on Earth or on other hydrated planetary surfaces like Mars. 相似文献
20.
Previous studies of the Green River kerogen only provide apparently contradictory conclusions about the size of the straight-chain aliphatic structures as well as the manner in which these structures form part of the kerogen matrix.The present investigation is an attempt to resolve this contradiction. A mild stepwise oxidation procedure was followed so that extensive degradation of kerogen-derived intermediates could be prevented. Products isolated from each oxidation step were analyzed by conventional GLC techniques, GC-MS, and proton-NMR measurements in order to ascertain the significance of the straight-chain aliphatic structures present in the Green River kerogen.The following results were obtained: (a) Green River kerogen contains a substantial portion (ca 2–4 carbons out of every 10) of straight-chain aliphatic structures which are longer than C4, (b) the kerogen matrix forms a three-dimensional network of non-straight-chain clusters interconnected by long polymethylene cross-links, (c) the ‘core’, in comparison with the ‘periphery’ of the kerogen matrix, contains a greater proportion of straight-chain and branched aliphatic structures which are attached to the kerogen matrix at one terminus, (d) some of the straight-chain structures may exist as physically entrapped components in the kerogen matrix. 相似文献