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1.
Macerals like sporinite, cutinite, suberinite and resinite of the liptinite group have been insufficiently recorded in Indian Permian Gondwana coals, until the fluorescence microscopy came into existence. With the introduction of this technique, macerals like bituminite, fluorinite and exsudatinite were convincingly recognized and alginite and liptodetrinite, normally mistaken for mineral matter under normal reflected light in routine coal petrographic analysis, were identified with certainty. Thus, fluorescence microscopy has added certain new macerals to the tally of the liptinite group and has increased their overall proportion in Indian Gondwana coals.In addition to the liptinite group, collodetrinite (=desmocollinite) and a certain fraction of collotelinite (=telocollinite) macerals of the vitrinite group were found to be fluorescing with dull reddish-brown to dark brown colours. Certain semifusinite and inertodetrinite macerals of inertinite group were also found to fluoresce with almost identical intensity and colour as that of the associated perhydrous (fluorescing) vitrinite. Contributions of degraded resinite, algal matter and bitumen in the formation of perhydrous vitrinite have been established. The fluorescence behaviour of inertinite appears to be related with its genesis from partial oxidation of resin/bitumen-impregnated cell walls.  相似文献   

2.
吐哈盆地侏罗纪煤中主要组分结构特征与生烃性分析   总被引:10,自引:0,他引:10  
在高纯度煤岩显微组分分离富集的基础上,应用透射式显微傅里叶红外光谱技术 (Micro FTIR),对吐哈盆地侏罗纪煤中的主要组分-镜质体、丝质体、角质体、藻类体的结构组成进行了测定。结果表明 :藻类体主要由长链脂族结构组成,芳香结构含量相对较少;角质体和基质镜质体中含有较丰富的芳香结构以及长链脂族结构;而丝质体则主要由芳香结构组成,脂族结构含量很少。显微组分的这种结构特征决定了藻类体具有很高的生烃潜力、角质体和镜质体的生烃潜力中等、而丝质体的生烃潜力则很低。对于吐哈盆地煤成油来说,由于藻类体主要由长链脂族结构组成,并且生烃潜力也高,因此其具有高的液态烃产率、丝质体的产油率最小、角质体和镜质体的液态烃产率中等。由于镜质体是本区煤中含量最高的组分。因此,对于吐哈盆地所形成的具有工业规模的油田来说,镜质体应该是主要的贡献组分之一。但对于富含藻类体的厚层状烛藻煤,由于它类型好,品质高、生烃潜力大、以中长链脂族结构为主,是煤成油最理想的源岩。  相似文献   

3.
从吐哈盆地侏罗纪煤中分离富集了藻类体、孢子体、角质体、镜质体、基质镜质体和丝质体6种主要显微组分,进行了热解及热模拟实验,并对各显微组分热模拟生成的产物热解油进行了碳同位素组成等分析。各显微组分热解生烃潜力及其热解产物热解油的碳同位素组成表明,煤系有机质中藻类体的生油潜力最高,生成的液态烃类的碳同位素组成最轻;孢子体、角质体等陆源富氢组分生烃潜力低于藻类体,生成的液态烃类的碳同位素组成重于藻类体生成的液态烃类,与煤系含油气盆地中原油的碳同位素组成基本一致。这些富氢显微组分应该是煤系有机质中主要的生油显微组分。镜质体和基质镜质体的生油潜力相对较低,其生成的液态烃类的碳同位素组成比一般煤系原油重得多,而且这些组分本身对液态烃具有较强的吸附力,尽管其在煤系有机质中所占的比例很大,仍然难以成为生成液态石油的主要显微组分,只能在高成熟演化阶段成为良好的生气显微组分。丝质体等惰性组分生烃潜力极低,不可能成为生油组分。此外,结合原煤的显微组分组成、生烃潜力和元素分析,提出仅仅以壳质组的含量高低来评价煤的生烃潜力不完全可靠,热解是经济、快速、有效的评价方法。  相似文献   

4.
This study describes changes of surface roughness of semifusinite and fusinite as an indicator of structural alteration resulting from heat treatment at 400–1200 °C. Surface roughness has been investigated by atomic force microscopy of inertinite concentrates from coking coals (vitrinite reflectance Rr = 1.07%–1.41%) from the Upper Silesian Coal Basin of Poland (Namurian C — Westphalian A). Unheated fusinite has a higher surface roughness than semifusinite from the same coal. The average surface roughness of semifusinite decreases with the Swelling Index of the parent coal. Heating increases the surface roughness of semifusinite and fusinite. Increase in the average surface roughness is stronger for semifusinite than fusinite and correlates to increasing reflectance of these macerals. The surface roughness of semifusinite correlates to the relative mass loss of the inertinite concentrates during heating. After heating to 1200 °C fusinite has a lower average surface roughness than semifusinite from the same coal. Consequently, average surface roughness can be used as a measure of structural alteration of inertinite group macerals during heat treatment.  相似文献   

5.
从西北地区侏罗纪煤中分离出来的不同显微组分热解油生物标志物总体上比较相似,但在一些特殊生物标志物的分布上存在明显差异。藻类体、孢子体、角质体热解油Pr/Ph比值一般在1.5~2.0之间,镜质体和基质镜质体热解油Pr/Ph比值在3~4之间,但均只有相应原煤抽提物Pr/Ph比值的一半。在常规生物标志物甾烷和萜烷组成中,藻类体和孢子体含有相对丰富的C27甾烷,角质体其次,镜质体和基质镜质体C27甾烷含量很低或者基本不含C27甾烷;藻类体和角质体含有较高的伽马蜡烷,而与藻类体来自相同原煤的孢子体伽马蜡烷含量很低;镜质体和基质镜质体基本上不含伽马蜡烷;分离显微组分的原煤伽马蜡烷含量均很低。由此可见,伽马蜡烷的含量不仅与有机质沉积水体的盐度有关,与母源的成分也有关系。显微组分热解油与煤系原油生物标志物组成特征对比表明,煤系原油是藻类体、孢子体、角质体等富氢组分和相对贫氢的镜质组生成产物的混合物。不同油气藏中的原油,每一类显微组分的贡献可能不尽相同,有些原油可能主要来源于藻类体和孢子体等富氢显微组分,而有些原油除了富氢显微组分有贡献外,镜质组对其也有一定的贡献,但富氢显微组分应该是煤系含油气盆地中主要的生油显微组分。  相似文献   

6.
The petrography of lignitic, subbituminous and bituminous inertinitic coals (i.e. coals containing > 30 modal percent inertinite on a mineral-matter-free basis) derived from limnic and paralic facies in the Upper Silesian coal basin of Poland was investigated. Paralic coals were observed to contain small amounts of telinite and abundant pyrofusinite compared to limnic coals. The ratio of oxysemifusinite and oxyfusinite to pyrosemifusinite and pyrofusinite is lower in paralic coals as compared to limnic coals. The statistical analysis of the reflectances of the inertinite group macerals and of vitrinite shows that paralic coals are more heterogeneous than limnic coals. This greater degree of heterogeneity may explain the differences in reactivity among coals that otherwise have the same rank and elemental and petrographic composition.  相似文献   

7.
鄂尔多斯盆地延安组煤有机岩石学研究   总被引:9,自引:1,他引:8  
鄂尔多斯盆地侏罗纪延安组煤系地层可否成为该盆地另一套油源岩的问题,历来存有争议。系统的煤岩和有机岩石学分析表明:煤中倾油性的壳质组分含量低,基质镜质体的类型也不利于生油,因此,延安组煤系有机质不大可能形成具有工业价值的煤成油藏  相似文献   

8.
Chars produced by the combustion of a set of three coals from Alberta, Canada, were classified morphologically using reflected light microscopy. Produced chars are different in morphological features, pore thickness, anisotropy and degree of reactivity, because of differences in the vitrinite and inertinite contents.The subbituminous A coal produced the highest percentage of unreactive or slightly reactive components due to its high inertinite content (20.0%), followed by isotropic cenospheres. Isotropic cenospheres, both thin- and thick-walled, and exploded cenospheres are the characteristic chars produced by the high-voltile bituminous B coal, whereas the low-volatile bituminous coking coal produced cenospheres with granular anisotropy (mosaic) on the walls and abundant coke fragmentsOptical microscopy is useful in differentiating the performance of a series of coals during combustion based on petrographic composition and rank and can aid in understanding the relationship between ‘reactive’ and ‘non-reactive’ coal macerals to burnout performance.  相似文献   

9.
《Chemical Geology》2006,225(1-2):77-90
Using density-gradient centrifugation, within-sample heterogeneity in C/N, δ13C, and δ15N was determined for a sample of the Blue Gem coal bed (Middle Pennsylvanian, Duckmantian (Westphalian B), Breathitt Formation) and related to maceral (petrographically identifiable organic component) composition. Relatively pure macerals were separated by density, with purities up to 99% in the case of vitrinite in fractions around 1.3 g/mL. Lower density fractions (∼ 1.2 g/mL) contain predominantly liptinite (∼ 75%) but also significant amounts of vitrinite (∼ 20%). Denser fractions contain increasing amounts of inertinite, with several fractions between 1.37 and 1.44 g/mL containing > 98% total inertinite. Within these denser fractions, semifusinite concentrated at lower densities than did fusinite. The separation of macerals by density allowed a more detailed evaluation of the isotopic composition of relatively pure macerals within a single coal. δ13C becomes increasingly heavy across the density gradient, with δ13C values being lightest in the liptinites, followed by vitrinite, and then semifusinite and fusinite; by contrast, δ15N becomes lighter across the same density range. C/H increases with density, reflecting a general decrease in aliphatic components and increase in aromatic components. C/N follows a similar pattern, ranging from < 40 to over 100, increasing significantly at densities > 1.32, the point at which inertinite macerals begin to predominate over vitrinite.The isotopic composition of macerals reflects chemical composition, which in turn reflects: 1) the original composition of plant tissues from which the macerals originated; 2) early diagenetic changes; and 3) changes during coalification. Macerals derived from lipid-rich precursor materials (liptinites) have more depleted δ13C values (∼ 2‰) relative to those derived from woody tissues (vitrinite). Fusinized material, derived from fossil charcoal, has δ13C values enriched by ∼ 0.5‰ compared with the vitrinite, consistent with the results from combustion experiments using modern plant tissues. Vitrinite fractions have enriched δ15N values relative to inertinite fractions, which may reflect early diagenetic changes in woody tissues involving preferential loss of 14N, possibly due to bacterial activity during the peat-forming stage. Due to the within-sample variability in carbon isotopic composition reported here, it is suggested that chemostratigraphic studies based on Type III kerogen (including both dispersed organic matter and coals) carefully consider the associated effects of variability in maceral composition.  相似文献   

10.
Petrographic analyses were carried out on thin coals and coaly sediments from the Lower Carboniferous Mattson Formation at Clausen Creek and Jackfish Gap-Yohin Ridge in the northern part of the Liard Basin, northern Canada. The composition and optical characteristics indicate that the coals are high-volatile bituminous B, predominantly sapropelic (canneloid) and accumulated subaquatically.The coals are dominantly composed of inertinite-rich and exinite-rich durities with subsidiary inertites and clarodurites; vitrite is minor and liptite is rare. The inertinite-rich microlithotypes are dominated by semifusinite, but micrinite, semimacrinite and ?resino-inertinites are abundant. Sporinite, comprising megaspores, crassispores, tenuispores and miospores, is the dominant liptinite maceral with subsidiary cutinite and minor alginite. Except for pyrite, mineral matter is minimal.Three populations of telocollinite are observed: a low-reflectance variety (I), commonly associated with micrinite (as vitrinertite), displays weak brown fluorescence and a reflectance some 0.4-0.5% lower than type II; type II is non-fluorescing telocollinite, with intermediate reflectance (0.67-0.74% Rom), it occurs as vitrite and is also associated with micrinite; and a higher-reflectance telocollinite (III), having no fluorescence or association with micrinite, has variable reflectance (0.74-0.8% Rom) implying higher oxidation or gelification levels.The abundance of semimacrinite, macrinite and ?resino-inertinites in inertites and durites (I) suggests that much of the peat accumulated subaquatically. Furthermore, fluorescing vitrinite and an abundance of micrinite (derived by oxidation or coalification of bituminite), suggest that the coal accumulated under anaerobic conditions. The predominance of semifusinite in humic laminae and micrinite in sapropelic layers suggests extensive surface or near-surface oxidation of the peat. Oxidised sporinites suggest that they were wind-borne.Depositional environment is interpreted as marginal marine, perhaps in shallow lakes in the middle to upper delta plain. Peat accumulations probably began subaquatically at the oxygen-hydrogen sulphide interface, but periodic subaerial exposure and natural oxidation gave rise to the high inertinite coals. Upper Mattson coals are interbedded with algal laminites and probably accumulated in a lagoonal setting.  相似文献   

11.
The effect of petrographic composition on the methane sorption capacity has been determined for a suite of coals and organic-rich shales. Subbituminous and bituminous coals were separated into bright and dull lithotypes by hand-picking. The methane sorption capacities range between 0.5 and 23.9 cm3/g at a pressure of 6 MPa. The low volatile bituminous Canmore coal and the anthracite sample have the highest capacities with the “natural coke” having the lowest. For low-rank coals there is no significant difference between bright and dull samples except for one coal with the dull sample having a greater sorption capacity than its bright equivalent. For higher-rank coals, the bright samples have a greater methane capacity than the dull samples and the difference between sample pairs increases with rank. The boghead coal samples have the highest sorption capacities in the liptinite-rich coals suite and are higher than subbituminous to medium volatile bituminous samples. Pore size distribution indicates that methane is held as solution gas in liptinite-rich coals and by physical sorption in micropores in liptinite-poor coals. These contrasting processes illustrate that liptinite-rich samples need to be independently assessed. The positive relationship between reactive inertinite content and methane sorption capacity occurs within the subbituminous to medium volatile bituminous coals because the reactive inertinite is structurally similar to vitrinite and have a higher microporosity than non-reactive inertinite. Reactivity of inertinite should be assessed in CBM studies of dull coals to provide a better understanding of petrographic composition effects on methane capacity.  相似文献   

12.
The Bolsovian (Middle Pennsylvanian) Peach Orchard coal bed is one of the splint coals of the Central Appalachians. Splint coal is a name for the dull, inertinite-rich lithologies typical of coals of the region. The No. 3 Split was sampled at five locations in Magoffin County, Kentucky and analyzed for petrography and major and minor elements. The No. 3 Split coals contain semifusinite-rich lithologies, up to 48% (mineral-free basis) in one case. The nature of the semifusinite varies with position in the coal bed, containing more mineral matter of detrital origin in the uppermost durain. The maceral assemblage of these terminal durains is dominated by detrital fusinite and semifusinite, suggesting reworking of the maceral assemblage coincident with the deposition of the detrital minerals. However, a durain in the middle of the coal bed, while lithologically similar to the uppermost durains, has a degraded, macrinite-rich, texture. The inertinite macerals in the middle durain have less distinct edges than semifusinites in the uppermost terminal durains, suggesting degradation as a possible path to inertinite formation. The uppermost durain has higher ash and semifusinite contents at the eastern sites than at the western sites. The difference in the microscopic petrology indicates that megascopic petrology alone can be a deceptive indicator of depositional environments and that close attention must be paid to the individual macerals and their implications for the depositional setting, especially within the inertinite group.  相似文献   

13.
The objective of the study was to characterize changes of reflectance, reflectance anisotropy and reflectance indicating surface (RIS) shape of vitrinite, sporinite and semifusinite subjected to thermal treatment under inert conditions. Examination was performed on vitrinite, liptinite and inertinite concentrates prepared from channel samples of steam coal (Rr = 0.70%) and coking coal (Rr = 1.25%), collected from seam 405 of the Upper Silesian Coal Basin. The concentrates were heated at temperatures of 400–1200 °C for 1 h time in an argon atmosphere.All components examined in this study: vitrinite, sporinite and semifusinite as well as matrix of vitrinite and liptinite cokes, despite of rank of their parent coal, show, in general, the most important changes of reflectance value and optical anisotropy when heated at 500 °C, 800 °C (with the exception of bireflectance value of sporinite) and 1200 °C.After heating the steam coal at 1200 °C, the vitrinite and the semifusinite reveal similar reflectances, whereas the latter a slightly stronger anisotropy. Sporinite and matrix of liptinite coke have lower reflectances but anisotropy (Rbi and Ram values) similar to those observed for vitrinite and semifusinite. However, at 1000 °C sporinite and matrix of liptinite coke have the highest reflectivity of the studied components. The RIS at 1200 °C is the same for all components.The optical properties of the three macerals in the coking coal become similar after heating at 1000 °C. Coke obtained at 1200 °C did not contain distinguishable vitrinite grains. At 1200 °C semifusinite and vitrinite coke matrix have highest Rr values among the examined components. Maximum reflectance (Rmax) reach similar values for vitrinite and sporinite, slightly lower for semifusinite. Matrix of liptinite coke and matrix of vitrinite coke have considerably stronger anisotropy (Rbi and Ram values) than other components. RIS at 1200 °C is also similar for all components.  相似文献   

14.
贵州水城煤中基质镜质体生烃潜力、烃类组成及生烃模式   总被引:3,自引:0,他引:3  
《沉积学报》2000,18(4)
基质镜质体是华南晚二叠世煤中的主要组分之一,其在煤中含量的多少、生烃潜力的大小、生烃特性等直接影响到该区煤成油气资源的评价。采用岩石热解、热解气相色谱以及开放体系下热模拟等方法,对贵州水城晚二叠世(R12)龙潭组煤中基质镜质体的生烃潜力、烃类组成特征、生烃模式进行了研究。结果表明:本区基质镜质体的生烃潜力、氢指数分别为191.99mg/g和250mg/gTOC,远高于丝质体的生烃潜力(26.17mg/g)和氢指数(35mg/gTOC),而小于树皮体的生烃潜力(297mg/g)和氢指数(491mg/gTOC);基质镜质体热解烃类组成中以轻质烃为主,湿气次之,可见本区基质镜质体不但能生成气态烃,而且能生成一定量的液态烃,这归因于其中所含大量的超微类脂体;基质镜质体“生油窗”温度范围为375~475℃,主要生烃温度区间为400~450℃,其中415~430℃为生烃高峰期,420℃处产烃率最高。基质镜质体这种在高成熟度下(大于VRo1.0%)大量生烃的特点对在成熟度普遍较高的华南地区寻找油气田具有重要的意义。  相似文献   

15.
吐哈盆地煤成烃主要贡献组分剖析   总被引:17,自引:4,他引:17  
吐哈盆地中下侏罗统煤显微组分组成显示了“碎、小、薄”和过渡组分含量高的特点。结合显微和超微层次有机岩石学分析,在显微组分层次生烃组分主要为基质镜质体,碎屑类脂体、薄壁角质体、木栓质体和小孢子体在煤成烃中也有一定的贡献;超微层次生烃组分主要表现为分布于基质镜质体中的超微类脂体。煤中基质镜质体的高含量弥补了其单位生烃潜力低的不足,基质镜质体富氢成因在于生物化学阶段细菌等微生物对其强烈降解改造作用。  相似文献   

16.
Seams from the St. Rose and Chimmey Corner coalfields, Nova Scotia, Canada, were sampled and examined for petrographic and geochemical composition. Rank determinations indicate a rank of high volatile C-B bituminous. Seams show regular alternations of dull and bright microbanded lithotypes, with dull lithotypes predominant in the central portion of the main seam (No. 5 seam). Brighter lithotypes are dominated by vitrinite (>80%), with minor inertinite (avg. 12%) and minor liptinite. Duller lithotypes contain greater amounts of inertinite (up to 40%) and liptinite (primarily sporinite). Mineral matter consists of epigenetic pyrite, with lesser amounts of clay and quartz. Cabonates are common in the Chimney Corner seams. Elemental composition of the seams is similar to other Canadian coals and fall within world coal ranges, with the exception of high concentrations of Cl, Zn, Ni, Mo, Pb, Cu and As.Depositional environment of the seams as indicated by maceral composition, lithotypes and geology suggest a predominance of wet forest to reed moor conditions, in a fluvial-lacustrine setting. Periodic episodes of flooding and drying are indicated by lithotype, maceral and mineral variations.  相似文献   

17.
The study was performed on inertinite concentrates prepared from 19 samples of bituminous, mostly coking, coal (Rr = 0.87–1.42%) from the Upper Silesian Coal Basin of Poland. In all examined samples, total semifusinite differs from fusinite, in terms of mean values, by higher frequencies of the D1 and D4 band position and lower frequency of the D3 band position, higher G band FWHM, the AD3/AALL and AD4/AALL ratios (where AALL means the surface of all the Raman bands), and lower D1 band FWHM, the ID1/IG and AD1/AALL ratios. Similar differences exist between reactive and non-reactive semifusinites. The diameter of coherent domains (La) increases in the following sequence: reactive semifusinite < non-reactive semifusinite < fusinite. The AD3 + D4/AALL ratio reflects inertinite reactivity in bituminous coals, and decreases with the increase of mean reflectance (Rr) of semifusinite and fusinite. Using the AD3 + D4/AALL, ID1/IG and AD1/AALL ratios or the D3 band position it is possible to interpret thresholds dividing, in terms of mean values, total semifusinite and fusinite, coming from different coals. The results of the study suggest that the term “semifusinite” should only comprise reactive and semi-reactive components. Non-reactive semifusinite should be considered fusinite. Semifusinite from bituminous coals (of Rr ≈ 0.9–1.4%), defined in the proposed way, would be characterized by the AD3 + D4/AALL ratio ≥ 0.35, or the ID1/IG ratio ≤ 1.03.  相似文献   

18.
孙旭光  金奎励 《沉积学报》2000,18(4):590-594
基质镜质体是华南晚二叠世煤中的主要组分之一,其在煤中含量的多少、生烃潜力的大小、生烃特性等直接影响到该区煤成油气资源的评价。采用岩石热解、热解气相色谱以及开放体系下热模拟等方法,对贵州水城晚二叠世(P21)龙潭组煤中基质镜质体的生烃潜力、烃类组成特征、生烃模式进行了研究。结果表明:本区基质镜质体的生烃潜力、氢指数分别为191.99mg/g和250mg/gTOC,远高于丝质体的生烃潜力(26.17mg/g)和氢指数(35mg/gTOC),而小于树皮体的生烃潜力(297mg/g)和氢指数(491mg/gTOC);基质镜质体热解烃类组成中以轻质烃为主,湿气次之,可见本区基质镜质体不但能生成气态烃,而且能生成一定量的液态烃,这归因于其中所含大量的超微类脂体;基质镜质体“生油窗”温度范围为375~475℃,主要生烃温度区间为400~450℃,其中415~430℃为生烃高峰期,420℃处产烃率最高。基质镜质体这种在高成熟度下(大于VRo1.0%)大量生烃的特点对在成熟度普遍较高的华南地区寻找油气田具有重要的意义。  相似文献   

19.
n-Alkanes in the soluble organic matter extracted from a series of vitrinite and sporinite concentrates have been analysed by gas chromatography. The macerals were isolated from coals ranging in rank from 77.1% to 86.6% carbon (vitrinite: dry, ash-free), and yields of n-alkanes ranged from 10 to 580 ppm for vitrinites and from 20 to 970 ppm for sporinites. The maximum yields were found at a rank of 85.4% C from vitrinites and 86.6% C from sporinites.Distribution maxima of the n-alkanes, as shown by gas chromatography, range from C27 and C29 at lower ranks to as low as C16 at higher ranks. The distributions also show a progressive decrease in the preference of odd-carbon-number homologues with increasing rank. Virtually smooth distributions were attained in high-volatile bituminous A coals. Quantitative data show that the loss of the odd-carbon-number preference occurred, for the most part, while individual long-chain homologues increased in concentration.There is a progressive increase in the amounts of shorter-chain n-alkanes with increasing rank. It is suggested that sequential processes may have occurred whereby the rate of formation of long-chain n-alkanes in high-volatile bituminous A rank macerals becomes slower than their rate of subsequent fragmentation to shorter chain lengths. Consequently, assuming derivation from the insoluble maceral matrices, the chain-length distributions of parent n-alkyl structures within the insoluble material may retain characteristics pertaining more to the nature of the source organic matter at the time of deposition than do the extractable n-alkane patterns, especially at higher ranks.  相似文献   

20.
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   

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