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1.
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   

2.
The molecular structure of an Eocene fossil resin (Vastan, Cambay basin, Western India) has been investigated with complimentary spectroscopic techniques. The FTIR spectrum shows strong aliphatic CH x (3000–2800 and 1460–1450 cm−1) and CH3 (1377 cm−1) absorptions and less intense aromatic C=C (1560–1610 cm−1) absorptions. The major products from analytical pyrolysis are cadalene based bicyclic sesquiterpenoids including some bicadinenes and bicadinanes. The polycadinane products confirm the fossil material as an Angiosperm dammar resin, associated with inputs of tropical rain forests supported by past climates.  相似文献   

3.
Micro-FTIR spectroscopy of liptinite macerals in coal   总被引：3，自引：0，他引：3  
Reflectance FTIR microspectroscopy has been used to investigate the chemical structure of the liptinite macerals, alginite, bituminite, sporinite, cutinite and resinite in bituminous coals of Carboniferous to Tertiary age. In comparison with the spectra of vitrinite in the same coals, the micro-FTIR spectra of liptinite macerals are characterized by stronger aliphatic CHx absorptions at 3000–2800 and 1460–1450 cm−1, less intense aromatic C=C ring stretching vibration and aromatic CH out of plane deformation at 1610–1560 and 900–700 cm−1 respectively and various intense acid C=O group absorptions at 1740–1700 cm−1. The peaks at 1000–900 cm−1 due to aliphatic CH2 wagging vibrations in olefins and at 730–720 cm−1 due to CH2 rocking vibration in long chain aliphatic substances ([CH2]n, n≥4), are characteristic of liptinite macerals. Collectively the micro-FTIR spectral characteristics indicate that liptinite is composed of greater numbers of long chain aliphatics, fewer aromatics and a broader range of oxygen-containing groups than other macerals. Marked differences exist in micro-FTIR spectra within the liptinite maceral group. Alginite has the strongest aliphatic and least aromatic absorptions followed by bituminite, resinite, cutinite and sporinite. The aliphatic components in alginite are the longest chained and least branched whereas those in sporinite are the shortest chained and most branched. Bituminite, resinite and cutinite are intermediate. Notable differences in micro-FTIR spectra of individual liptinite macerals, such as intensities and peak locations of aromatic C=C in alginite, C=O groups in bituminite and resinite and substituted aromatic CH and C–O–C groups in cutinite and sporinite, also exist, which are attributed to differences in depositional environments or biotaxonomy.  相似文献   

4.
Immature vitrinite samples from a Miocene lignite seam of western Germany (H/C = 1.14, O/C = 0.41) and alginite concentrates from a Tasmanite deposit of Australia (H/C = 1.60, O/C = 0.10) were pyrolyzed in a stream of argon at heating rates of 0.1 and 2.0°C/min up to temperatures varying from 200 to 670°C. The solid maceral residues were subjected to elemental and microscopical analysis and studied by IR and 13C CP/MAS NMR spectroscopy with respect to structural modifications.The maximum pyrolytic weight loss amounts to 60% of the initial organic matter in the case of vitrinite and to 85% for alginite, the onset of degradation reactions being shifted to higher temperatures with increasing rate of heating. Both infrared and NMR spectra of the vitrinite samples indicate a rapid decomposition of the cellulose component upon heating whereas lignin related structures such as aromatic ether linkages remain remarkably stable. The main hydrocarbon release from vitrinite occurs at very early evolution stages (Tmax = 296°C, Rm = 0.20% at 0.1°C/min; Tmax = 337°C, Rm = 0.23 at 2.0°C/min). Hydrocarbon generation from alginite requires higher temperatures (Tmax = 388 and 438°C) and is completed within a distinctly narrower temperature range.The pronounced increase of vitrinite reflectance between 350 and 670°C seems to be associated with a rather time-consuming reorganization of the residual organic material. The concomitant growth of polyaromatic units is illustrated by the increasing intensity ratio of the aromatic ring stretching vibration bands at 1600 and 1500 cm−1. These reactions are moreover marked by increasing loss of phenolic oxygen and by increasing conversion of aliphatic carbon into fixed aromatic carbon.  相似文献   

5.
This paper entails the results of the investigations undertaken to assess the oil potential of two lignite deposits, Rajpardi and Vastan, from Gujarat, western India. They are ‘Low rank B’ type lignite. Petrographically, they are enriched in huminite and are low in liptinite and inertinite. Their elevated hydrogen content, in relation to carbon, has probably made them perhydrous in nature and oil prone. The reactivity of these coals during liquefaction has also been discussed in the light of petrofactor. Good correlation has been noticed between oil yield and conversion (r2 = 0.999) in both the lignite deposits. The VRr (0.24–0.35% in both lignites), H/C atomic ratio (0.11–1.39 in Rajpardi and 1.09–1.88 in Vastan), reactive maceral content (91.6–99.8 vol % mmf in Rajpardi lignite and 75.5–99.7 vol % in Vastan lignite) and VMdaf (64.8–67.9 wt % in Rajpardi lignite and 42.1–80.0 wt % in Vastan lignite) of these lignites have a favourable range required for a coal to generate oil. Huminite is seen to play a vital role in conversion and maintains a good correlation with it. The calculations show that these lignites have a high conversion (> 95%) and oil yield (> 65%).  相似文献   

6.
《地学前缘(英文版)》2020,11(3):965-988
The sedimentary sequence containing lignite deposits in Gurha quarry of the Bikaner-Nagaur Basin(Rajasthan)has been investigated.The samples from lignite and allied shale horizons were evaluated for petrographical,palynological,palynofacies and organic geochemical inferences,to depict the source flora and to reconstruct the palaeodepositional conditions prevailed during the sedimentation.An assessment for the hydrocarbon generation potential of these deposits has also been made.The results revealed the dominance of huminite macerals and phytoclasts organic matter(OM) indicating the existence of forested vegetation in the vicinity of the depositional site.A relatively high terrigenous/aquatic ratio(TAR) and the carbon preference index(CPI) are also suggesting the contribution of higher plants in the peat formation.However,the n-alkane distributions,maximizing at n-C17 and n-C29,showed inputs from the algal communities along with the higher plant derived organic matters.Recovered palynomorphs of the families Onagraceae,Meliaceae,Arecaceae,Rhizophoraceae,Rubiaceae,Ctenolophonaceae, etc.together with oleanene and ursane types of triterpenoids suggest the contribution from angiosperms source vegetation.Interestingly,the presence of Araucareaceae and Podocarpaceae pollen grains shows the existence of gymnosperms vegetation.Further,the presence of tetracyclic diterpanes;demethylated entbeyerane,sandaracopimarane,pimarane,and Kaurane type of compounds confirms the contribution of conifers.The variation in the values of the coefficient of non-equality(H:0.68%-7.56%),the standard deviation(8:0.04%-0.16%) and the coefficient of variability(V:16.10%-46.47%),also shows the heterogeneity in the source organic matter.The various petrographical indices,palynological entities,and geochemical parameters indicate that the peatforming vegetation was accumulated under a mixed environment and fluctuating hydrological settings.The interpretation of palynofacies data on APP(Amorphous organic matter-Phytoclast-Palynomorphs) diagram suggests that the accumulation of organic matter occurred in a dysoxic-suboxic condition in a proximal(to land)setting with the shift to an anoxic condition in distal setting towards the termination of sedimentation.The huminite(ulminite) reflectance(R_r) values(av.0.28%) showed a good relationship with average T_(max) value(414℃),suggesting the immaturity.The TOC content ranges of 13-59 wt.%,and HI values vary between 101 and 546 mg HC/g TOC in the studied samples.Collectively,the studied lignite and shale samples have the admixed kerogens(Type Ⅲ-Ⅱ) and exhibit the ability to generate the gaseous to oil hydrocarbons upon maturation.  相似文献   

7.
FT-IR and XRD analysis of coal from Makum coalfield of Assam   总被引：1，自引：0，他引：1  
High sulphur coal sample from Ledo colliery of Makum coalfield, Assam, India was studied using FT-IR and XRD methods. FT-IR study shows the presence of aliphatic -CH, -CH2 and -CH3 groups, aliphatic C-O-C stretching associated with -OH and -NH stretching vibrations and HCC rocking (single and condensed rings). XRD pattern of the coal shows that it is amorphous in nature. Function of Radial Distribution Analysis (FRDA) indicates that coal is lignite in type and there is no evidence of graphite-like structure. The first maximum in the G(r) plot of FRDA at r = 0.14 nm relates to the aliphatic C-C bond (Type C-CH=CH-C), the second maximum at r = 0.25 nm relates to the distance between carbon atoms of aliphatic chains that are located across one carbon atom. The curve intensity profiles obtained from FRDA show quite regular molecular packets for this coal. The coal was found to be lignite in nature.  相似文献   

8.
The cuticles and cuticle-free compressions of three Carboniferous medullosan seed-fern leaf species (Macroneuropteris scheuchzeri, Neuropteris ovata var. simonii and Alethopteris lesquereuxii) were analyzed by elemental, 13C nuclear magnetic resonance (NMR), micro-FTIR (Fourier transform infrared) and coal petrographic techniques. The 13C NMR spectra of the cuticle-free compressions and the associated whole coal (high volatile A/B bituminous coal rank) are generally similar and consist of a large aromatic carbon peak, a smaller aliphatic carbon peak and a shoulder on the aromatic peak, representing phenolic carbons. In contrast, the 13C NMR spectra of the cuticles from the same leaves have a predominant peak for aliphatic carbons and a much smaller aromatic carbon peak. This difference in aromaticity between the cuticles and the cuticle-free compressions is also reflected in the higher atomic H/C ratios of the cuticles. Micro-FTIR spectra of the cuticles show oxygenated functional groups (carboxyl and ketone) similar to those in modern cuticles but their most characteristic feature is very strong bands in the aliphatic stretching region. The cuticle-free compressions (mainly vitrinite), in turn, show the absence or significant reduction in oxygenated functional groups, reduction in aliphatic stretching bands and, usually, increased absorbance of aromatic out-of-plane deformation in the 700–900 cm−1 region. Fluorescence spectra for the cuticles from all three species show a great similarity with a λmax at 580–590 nm, probably reflecting a similardegree of coalification, which is consistent with the similar vitrinite reflectance (Rr) and H/C and O/C ratios of the cuticlefree compressions.These results indicate that leaf cuticle-free compressions, which were initially cellulose rich ( 90% cellulose and hemicellulose, < 10% lignin), can alter, during peatification and coalification, to a macromolecular structure similar to that of coalified wood (initially 50% cellulose and hemicellulose, 30%–50% lignin). Thus, a lignin-enriched structure is not a prerequisite for the formation of the macromolecular structure of vitrinite. In addition, the micro-FTIR spectra reveal the complexity of the molecular structure in coalified seed-fern leaves. The micro-FFIR data reveal some significant differences among the cuticles that may be of chemotaxonomic value. Clearly, a combination of macro- and micro-techniques offers a better basis for the interpretation of the molecular structure of pre-macerals and their alteration during peatification and coalification. Also, the data presented in this paper provide important new information that extends the data from morphological and cuticular taxonomic studies of some seed ferns. The data are encouraging preliminary advances in the chemotaxonomy of medullosan seed fern species.Pyrolysis-gas chromatography (PY-GC) data for the cuticles of three seed-fern leaves indicate distinct chemical signatures for the two neuropterid leaves as compared to the Alethopteris leaf. This perhaps indicates a chemotaxomic factor, or it could be related to the greater thickness of the cuticle of Alethopteris. Mass spectrometric data are needed to identify individual components in the PY-GC chromatograms.  相似文献   

9.
Five of the most important Colombian coals were studied using Photoacoustic Fourier transform infrared (PA-FTIR) spectroscopy. The PA-FTIR spectra were used to obtain structural parameters and to determine the analytical potential of this technique. The molecular structural parameters, CH2/CH3, fa, Hal/Har, and (R/C)u were correlated with fixed carbon contained in the samples to determine aliphatic hydrogen, Hal, and the aromatic hydrogen, Har in coals studied here. These parameters enabled the determination of aromaticity, fa, which was found to be between 0.66 and 0.98. The aliphatic and aromatic regions were considered between 3005–2760 cm?1 and 912–670 cm?1, respectively. Finally, using the molecular structural parameters, the grade of maturation (rank) of coal samples studied was determined.  相似文献   

10.
 Cordierite precursors were prepared by a sol-gel process using tetraethoxysilane, aluminum sec.-butoxide, and Mg metal flakes as starting materials. The precursors were treated by 15-h heating steps in intervals of 100 °C from 200 to 900 °C; they show a continuous decrease in the analytical water content with increasing preheating temperatures. The presence of H2O and (Si,Al)–OH combination modes in the FTIR powder spectra prove the presence of both H2O molecules and OH groups as structural components, with invariable OH concentrations up to preheating temperatures of 500 °C. The deconvolution of the absorptions in the (H2O,OH)-stretching vibrational region into four bands centred at 3584, 3415, 3216 and 3047 cm−1 reveals non-bridging and bridging H2O molecules and OH groups. The precursor powders remain X-ray amorphous up to preheating temperatures of 800 °C. Above this temperature the precursors crystallize to μ-cordierite; at 1000 °C the structure transforms to α-cordierite. Close similarities exist in the pattern of the 1400–400 cm−1 lattice vibrational region for precursors preheated up to 600 °C. Striking differences are evident at preheating temperatures of 800 °C, where the spectrum of the precursor powder corresponds to that of conventional cordierite glass. Bands centred in the “as-prepared” precursor at 1137 and 1020 cm−1 are assigned to Si–O-stretching vibrations. A weak absorption at 872 cm−1 is assigned to stretching modes of AlO4 tetrahedral units and the same assignment holds for a band at 783 cm−1 which appears in precursors preheated at 600 °C. With increasing temperatures, these bands show a significant shift to higher wavenumbers and the Al–O stretching modes display a strong increase in their intensities. (Si,Al)–O–(Si,Al)-bending modes occur at 710 cm−1 and the band at 572 cm−1 is assigned to stretching vibrations of AlO6 octahedral units. A strong band around 440 cm−1 is essentially attributed to Mg–O-stretching vibrations. The strongly increasing intensity of the 872 and 783 cm−1 bands demonstrates a clear preference of Al for a fourfold-coordinated structural position in the precursors preheated at high temperatures. The observed band shift is a strong indication for increasing tetrahedral network condensation along with changes in the Si–O and Al–O distances to tetrahedra dimensions similar to those occurring in crystalline cordierite. These structural changes are correlated to the dehydration process starting essentially above 500 °C, clearly demonstrating the inhibiting role of H2O molecules and especially of OH groups. Received: 1 March 2002 / Accepted: 26 June 2002  相似文献   

11.
In this study, attenuated total reflectance (ATR) Fourier transform infrared spectroscopy (FTIR) was coupled with partial least squares regression (PLSR) analysis to relate spectral data to parameters from total organic carbon (TOC) analysis and programmed pyrolysis to assess the feasibility of developing predictive models to estimate important organic geochemical parameters. The advantage of ATR-FTIR over traditional analytical methods is that source rocks can be analyzed in the laboratory or field in seconds, facilitating more rapid and thorough screening than would be possible using other tools. ATR-FTIR spectra, TOC concentrations and Rock–Eval parameters were measured for a set of oil shales from deposits around the world and several pyrolyzed oil shale samples. PLSR models were developed to predict the measured geochemical parameters from infrared spectra. Application of the resulting models to a set of test spectra excluded from the training set generated accurate predictions of TOC and most Rock–Eval parameters. The critical region of the infrared spectrum for assessing S1, S2, Hydrogen Index and TOC consisted of aliphatic organic moieties (2800–3000 cm−1) and the models generated a better correlation with measured values of TOC and S2 than did integrated aliphatic peak areas. The results suggest that combining ATR-FTIR with PLSR is a reliable approach for estimating useful geochemical parameters of oil shales that is faster and requires less sample preparation than current screening methods.  相似文献   

12.
Thermally metamorphosed Tertiary age coals from Tanjung Enim in South Sumatra Basin have been investigated by means of petrographic, mineralogical and chemical analyses. These coals were influenced by heat from an andesitic igneous intrusion. The original coal outside the metamorphosed zone is characterized by high moisture content (4.13–11.25 wt.%) and volatile matter content (> 40 wt.%, daf), as well as less than 80 wt.% (daf) carbon and low vitrinite reflectance (VRmax = 0.52–0.76%). Those coals are of subbituminous and high volatile bituminous rank. In contrast the thermally metamorphosed coals are of medium-volatile bituminous to meta-anthracite rank and characterized by low moisture content (only < 3 wt.%) and volatile matter content (< 24 wt.%, daf), as well as high carbon content (> 80 wt.%, daf) and vitrinite reflectance (VRmax = 1.87–6.20%). All the studied coals have a low mineral matter content, except for those which are highly metamorphosed, due to the formation of new minerals.The coalification path of each maceral shows that vitrinite, liptinite and inertinite reflectance converge in a transition zone at VRmax of around 1.5%. Significant decrease of volatile matter occurs in the zone between 0.5% and 2.0% VRmax. A sharp bend occurs at VRmax between 2.0% and 2.5%. Above 2.5%, the volatile matter decreases only very slightly. Between VRr = 0.5% and 2.0%, the carbon content of the coals is ascending drastically. Above 2.5% VRr, the carbon content becomes relatively stable (around 95 wt.%, daf).Vitrinite is the most abundant maceral in low rank coal (69.6–86.2 vol.%). Liptinite and inertinite are minor constituents. In the high rank coal, the thermally altered vitrinite composes 82.4–93.8 vol.%. Mosaic structures can be recognized as groundmasss and crack fillings. The most common minerals found are carbonates, pyrite or marcasite and clay minerals. The latter consist of kaolinite in low rank coal and illite and rectorite in high rank coal. Change of functional groups with rank increase is reflected most of all by the increase of the ratio of aromatic C–H to aliphatic C–H absorbances based on FTIR analysis. The Oxygen Index values of all studied coals are low (OI < 5 mg CO2/g TOC) and the high rank coals have a lower Hydrogen Index (< 130 mg HC/g TOC) than the low rank coals (about 300 mg HC/g TOC). Tmax increases with maturity (420–440 °C for low rank coals and 475–551 °C for high rank coals).Based on the above data, it was calculated that the temperature of contact metamorphism reached 700–750 °C in the most metamorphosed coal.  相似文献   

13.
To study the detailed structural and isotopic heterogeneity of the insoluble organic matter (IOM) of the Murchison meteorite, we performed two types of pyrolytic experiments: gradual pyrolysis and stepwise pyrolysis. The pyrolysates from the IOM contained 5 specific organic groups: aliphatic hydrocarbons, aromatic hydrocarbons, sulfur-bearing compounds, nitrogen-bearing compounds, and oxygen-bearing compounds. The release temperatures and the compositions of these pyrolysates demonstrated that the IOM is composed of a thermally unstable part and a thermally stable part. The thermally unstable part mainly served as the linkage and substituent portion that bound the thermally stable part, which was dispersed throughout the IOM. The linkage and substituent portion consisted of aliphatic hydrocarbons from C4 to C8, aromatic hydrocarbons with up to 6 rings, sulfo and thiol groups (the main reservoirs of sulfur in the IOM), and carboxyl and hydroxyl groups (the main reservoirs of oxygen). However, the thermally stable part was composed of polycyclic aromatic hydrocarbons (PAHs) containing nitrogen heterocycles in the IOM. Isotopic data showed that the aliphatic and aromatic hydrocarbons in the linkage and substituent portion were rich in D and 13C, while the thermally stable part was deficient in D and 13C. The structural and isotopic features suggested that the IOM was formed by mixing sulfur- and oxygen-bearing compounds rich in D and 13C (e.g., polar compounds in the interstellar medium (ISM)) and nitrogen-bearing PAHs deficient in D and 13C (e.g., polymerized compounds in the ISM).  相似文献   

14.
Insoluble organic matter (IOM) isolated from 22 carbonaceous and ordinary chondrites spanning a wide range of groups and petrologic types were analyzed using Fourier transform infrared spectroscopy (FTIR). Based on common IR spectral features, it is observed that IOM falls into 4 molecularly distinct groups (designated here as A through D). Spectral group A includes type 1 and 2 chondrites and exhibits intense aliphatic C-H and carboxyl vibrational peaks. Spectral group B includes the least metamorphosed type 3 chondrites and Tagish Lake, and exhibits weaker aliphatic and carboxyl vibrational intensity. Spectral groups C and D include metamorphosed type ?3.1 chondrites and a heated CM chondrite. The carbonyl stretching features in spectral groups C and D differ from that in spectral groups A and B and from each other. In spectral group C, the carbonyl stretching is assigned to cyclic unsaturated lactones; in spectral group D carbonyl exists predominantly in the form of unsaturated ketone moieties. Both spectral groups C and D have a relatively narrow band structure around 1210 cm−1 (assigned to aromatic skeletal modes) as compared with spectral groups A and B, which is consistent with the formation of more condensed aromatics by extensive thermal metamorphism. The differences in carbonyl structures in spectral groups C and D are not the result of different effective metamorphic temperatures, rather these differences likely result from variation in the activity of water and oxygen at different stages of parent body metamorphism. Such environmental variations must be local phenomena in the parent bodies as there is no correlation between spectral grouping and chondrite class or group.  相似文献   

15.
The polarized Raman spectra of four different beryl crystals were studied at room temperature in the range from 30 to 4000 cm-1. The spectra show significant differences between the samples studied, and corrections are proposed for the reference Raman spectra of beryl previously reported by Adams and Gardner (1974). Type II water is observed in two crystals; the corresponding symmetric Raman stretching band at 3595 cm-1 is extremely strong for an impurity (about 20% of the strongest beryl lattice mode). Another, sharper, band of similar intensity at 3605 cm-1 could possibly originate from a hydroxyl stretching mode. Additional weaker bands are observed around 1600 cm-1 and 3600–3750 cm-1. The first polarized Raman spectra of bazzite are presented and discussed.  相似文献   

16.
The southern Bida Basin in central Nigeria forms a part of the larger Bida or Middle Niger Basin, which is contiguous with the south east trending (petroliferous) Anambra Basin. These basins were major depocenters for Campanian–Maastrichtian sediments in southern and central Nigeria prior to the build up of the Tertiary Niger delta. The successions in the southern Bida Basin consist of the basal Lokoja Formation, overlain by the Patti Formation and capped by the Agbaja Formation. The Lokoja Formation is a sequence of matrix supported conglomerates and sandstones overlying the Pre-Cambrian to Lower Paleozoic basement. Depositional environments are predominantly within fluvial systems of a continental setting. The Patti Formation consists of dark grey carbonaceous shales; mudstone and siltstones representing flood plains to shallow marine deposits with likely organic rich intervals. The overlying Agbaja Formation is made up of ferruginised oolitic and kaolinitic mudstone of a marginal marine environment. Twenty samples of shales of the Patti Formation were studied by incident light microscopy and geochemical analysis to determine the maceral components, geochemical type and potential yield of the pyrolysate. Maceral analysis indicate a large abundance of vitrinite (50–85%; mean = 66%); moderate abundance of liptinites (10–33%; mean = 18%) and lesser amounts of inertinite (9–40%; mean = 16%). Total organic carbon (TOC) values vary from 0.17 to 3.8 wt.% (mean = 2.1 wt.%) with most samples having greater than 2 wt.% TOC. Three of the samples yield greater than 2 kg(HC)/ton of rock suggesting a fair source rock potential. Most of the samples are thermally immature to marginally mature with vitrinite reflectance ranging from 0.4 to 0.6% Rom and Tmax values of 407–426 °C. Given the prevalence of the humic Type III kerogen, maturity and hydrocarbon potential yields, we conclude that the Patti Formation source rock facies have moderate to fair potential for gaseous hydrocarbons which have not yet been generated at the present day outcrop levels but could be important gas source where buried down-dip.  相似文献   

17.
安徽马鞍山磷铝石宝石矿物学特征研究   总被引：3，自引：1，他引：2  
周彦  亓利剑  戴慧  张青  蒋小平 《岩矿测试》2014,33(5):690-697
近年来在安徽马鞍山地区所在的绿松石矿体附近,相继发现一种绿色、半透明的磷铝石,部分达到宝石级别。本文采用电子探针、X射线粉晶衍射仪、扫描电镜、傅里叶变换红外光谱仪、紫外可见光谱仪等测试技术,对该地区磷铝石的化学成分、矿物成分、微观结构和光谱特征进行对比验证和综合分析,研究其水的赋存形式,进而对磷铝石的呈色机制作了深入探讨。电子探针分析显示该地区磷铝石的化学成分主要以Al、P元素组成,含微量的Fe、V元素。X射线粉晶衍射与红外吸收光谱分析表明主要矿物为磷铝石,基本不含有其他杂质矿物;磷铝石是一种水合磷酸盐矿物,含有结晶水以及少量结构水的矿物,且结晶水与结构水多与Al3+(Fe3+)相结合的形式存在。偏光显微镜和扫描电镜观察显示磷铝石整体以鳞片状集合体产出,微观上多以短柱状及板片状堆积,单个晶体显示斜方晶系结晶生长习性。紫外可见吸收光谱中639 nm处吸收谱峰由Fe3+与V3+联合所致,300、423、864 nm处吸收峰由Fe3+所致,说明Fe3+与V3+的共同作用是马鞍山地区磷铝石呈现绿色的主要原因。本研究对于认识该类磷铝石的宝石矿物学性质以及颜色成因具有一定意义。  相似文献   

18.
The composition of humic acids (HAs) isolated from an agricultural soil and a lignite deposit was examined via H2O2 and RuO4 oxidation. The oxidation digests were separated into lipophilic and hydrophilic components. Information with regard to the source, degree of humification and preservation of easily degradable constituents of the HAs was obtained and results were compared with those obtained earlier for base hydrolysates of solvent-extracted fractions.H2O2 oxidation of both HAs afforded lipophilic fractions containing high molecular weight compounds. The composition of the base hydrolysates of the lipophilic fractions strongly differed with the origin of the HA. The lipophilic components of the soil HA derived mainly from the higher plant polyesters cutin and suberin. The lipophilic components of the lignite HA predominantly comprised long chain alkanoic acids and alkanols. The patterns for the hydrophilic components released upon H2O2 oxidation were found to be identical irrespective of the origin of the HA. The hydrophilic fractions comprised aliphatic (poly)carboxylic acids related to carbohydrate moieties and benzene polycarboxylic acids. The relative abundance of benzene polycarboxylic acids increased with the degree of humification.For both HAs, RuO4 oxidation resulted in a lipophilic fraction containing low molecular weight products identical to those found in the base hydrolysate of the lipophilic fraction released upon H2O2 oxidation. The hydrophilic components released upon RuO4 oxidation were independent of the HA origin and consisted mainly of monosaccharides and disubstituted aromatic compounds. In agreement with the greater aromaticity of lignite HA, the aromatic compound/carbohydrate ratio was higher for lignite HA than soil HA. The results show that the fused aromatic structures had a small size and that carbohydrates could escape degradation during the humification process.  相似文献   

19.
Solid-state 1H and 13C Nuclear Magnetic Resonance (NMR) spectroscopic experiments have been performed on isolated meteoritic Insoluble Organic Matter (IOM) spanning four different carbonaceous chondrite meteorite groups; a CR2 (EET92042), a CI1 (Orgueil), a CM2 (Murchison), and the unique C2 meteorite, Tagish Lake. These solid state NMR experiments reveal considerable variation in bulk organic composition across the different meteorite group’s IOM. The fraction of aromatic carbon increases as CR2 < CI1 < CM2 < Tagish Lake. The increases in aromatic carbon are offset by reductions in aliphatic (sp3) carbon moieties, e.g., “CHx,” and “CHx(O,N).” Oxidized sp2 bonded carbon, e.g., carboxyls and ketones grouped as “CO,” are largely conservative across these meteorite groups. Single pulse (SP) 13C magic angle spinning (MAS) NMR experiments reveal the presence of nanodiamonds with an apparent concentration ranking in the IOM of CR2 < CI1 < CM2 < Tagish Lake. A pair of independent NMR experiments reveals that, on average, the aromatic moieties in the IOM of all four meteoritic IOM fractions are highly substituted. Fast spinning SP 1H MAS NMR spectral data combined with other NMR experimental data reveal that the average hydrogen content of sp3 bonded carbon functional groups is low, requiring a high degree of aliphatic chain branching in each IOM fraction. The variation in chemistry across the meteorite groups is consistent with alteration by low temperature chemical oxidation. It is concluded that such chemistry principally affected the aliphatic moieties whereas the aromatic moieties and nanodiamonds may have been largely unaffected.  相似文献   

20.
Abstract

Small- and medium-sized basins are widely distributed, and some contain commercial gas reservoirs demonstrating their gas-generation potential. The Xuanhua Basin, which is a small-sized coal-bearing basin in north China, includes a promising target for shale-gas exploration in the Xiahuayuan Formation. In this study, we used this basin as a case study to assess the critical geochemical features for small or medium-sized basins to form commercial gas reservoirs. Total organic carbon (TOC) analysis, Rock-Eval pyrolysis, microscopic observation of macerals, vitrinite reflectance measurement and kerogen stable carbon isotope analysis were performed to characterise the organic geochemistry of the Xiahuayuan shales. The original total organic carbon (TOCo) content and hydrocarbon-generative potential (S2o) were reconstructed to further evaluate the gas-generation potential of these shales. In addition, geochemical data of shales from other similar-sized basins with gas discoveries were compared. The results showed that the kerogen from the Xiahuayuan Formation is Type III (gas-prone), and macerals are dominated by vitrinite. TOC values showed a strong heterogeneity in the vertical profiles, with most higher than 1.5?wt%. The measured Ro values ranged from 1.4 to 2.0%. However, thermal maturity was not correlated with the present-day burial depth with higher maturity in the wells closest to the diabase intrusion centre. The remaining generation potential (S2) averaged 0.91?mg HC/g rock, equal to 1.4?cm3 CH4/g rock, and the average amount of hydrocarbon generated was 4.33?cm3 CH4/g rock. In small and medium-sized basins, the TOC content of commercially developed gas shales ranged from 0.5 to 2.5?wt%, organic matter was mainly humic (gas-prone), and the burial depth was generally shallow. Biogenic gas reservoirs for commercial exploitation tend to have larger shale thicknesses (120–800?m) than thermogenic gas reservoirs (60–90?m).

  1. The Xiahuayuan Formation is a good gas-source rock with gas-prone kerogen type, relatively high TOC values and moderate thermal maturity.

  2. The average amount of hydrocarbon generated from the Xiahuayuan shales is about 4.33?cm3 CH4/g rock, indicating a potential to form a shale gas reservoir.

  3. Owing to the influence of diabase intrusions, the Xiahuayuan shales have entered the dry gas window at relatively shallow-buried depths.

  4. Small- and medium-sized basins have the potential to generate commercial gas reservoirs with the generated volume mainly a product of the thickness and maturity of black shales.

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