The petroleum generation potential and effective oil window of humic coals related to coal composition and age   总被引：1，自引：0，他引：1  

Henrik I. Petersen   《International Journal of Coal Geology》2006,67(4):221-248

A worldwide data set of more than 500 humic coals from the major coal-forming geological periods has been used to analyse the evolution in the remaining (Hydrogen Index, HI) and total (Quality Index, QI) generation potentials with increasing thermal maturity and the ‘effective oil window’ (‘oil expulsion window’). All samples describe HI and QI bands that are broad at low maturities and that gradually narrow with increasing maturity. The oil generation potential is completely exhausted at a vitrinite reflectance of 2.0–2.2%R_o or T_max of 500–510 °C. The initial large variation in the generation potential is related to the original depositional conditions, particularly the degree of marine influence and the formation of hydrogen-enriched vitrinite, as suggested by increased sulphur and hydrogen contents. During initial thermal maturation the HI increases to a maximum value, HI_max. Similarly, QI increases to a maximum value, QI_max. This increase in HI and QI is related to the formation of an additional generation potential in the coal structure. The decline in QI with further maturation is indicating onset of initial oil expulsion, which precedes efficient expulsion. Liquid petroleum generation from humic coals is thus a complex, three-phase process: (i) onset of petroleum generation, (ii) petroleum build-up in the coal, and (iii) initial oil expulsion followed by efficient oil expulsion (corresponding to the effective oil window). Efficient oil expulsion is indicated by a decline in the Bitumen Index (BI) when plotted against vitrinite reflectance or T_max. This means that in humic coals the vitrinite reflectance or T_max values at which onset of petroleum generation occurs cannot be used to establish the start of the effective oil window. The start of the effective oil window occurs within the vitrinite reflectance range 0.85–1.05%R_o or T_max range 440–455 °C and the oil window extends to 1.5–2.0%R_o or 470–510 °C. For general use, an effective oil window is proposed to occur from 0.85 to 1.7%R_o or from 440 to 490 °C. Specific ranges for HI_max and the effective oil window can be defined for Cenozoic, Jurassic, Permian, and Carboniferous coals. Cenozoic coals reach the highest HI_max values (220–370 mg HC/g TOC), and for the most oil-prone Cenozoic coals the effective oil window may possibly range from 0.65 to 2.0%R_o or 430 to 510 °C. In contrast, the most oil-prone Jurassic, Permian and Carboniferous coals reach the expulsion threshold at a vitrinite reflectance of 0.85–0.9%R_o or T_max of 440–445 °C.  相似文献   

Transformation of arsenic compounds in modern intertidal sediments of Iriomote Island, Japan   总被引：1，自引：0，他引：1  

Harue Masuda  Yoshito Yamatani  Mitsuru Okai   《Journal of Geochemical Exploration》2005,87(2):587-81

The arsenic accumulation process in intertidal sediments of Iriomote Island, Japan, is analyzed as a naturally balanced arsenic-fixation system. Major and minor element chemistry is analyzed by X-ray fluorescence photometry, mineralogy is investigated by X-ray diffractometry, and four arsenic compounds are characterized by hydrogen-generated atomic absorption photometry. It is found that arsenic is accumulated by iron hydroxides/oxides precipitated following the decomposition of humic acids in the shallower sediment, and is subsequently incorporated into iron sulfide minerals at depth. The arsenic is immobile during incorporation into arsenic-bearing phases, suggesting that arsenic is unlikely to be released into the porewater under natural conditions in early diagenesis. The formation and decomposition of arsenic-bearing organic compounds appear to be associated with the formation and decomposition of arsenic in oxyhydroxides/oxides, suggesting that microbial activity may play an important role in controlling the behavior of arsenic and arsenic-bearing phases in the sediment column.  相似文献   

Sunlight Degradation of Aquatic Humic Substances Abbau von Huminstoffen unter dem Einfluß von Sonnenlicht     

D. Hongve 《洁净——土壤、空气、水》1994,22(3):117-120

Coloured bog water and an aqueous solution of fulvic acid were exposed to natural sunlight. Up to 67% reduction in colour and 32% reduction in DOC concentration were measured after 12 days exposure. Colour bleaching and reduction in ultraviolet light absorbance were independent of added preservatives. The high molecular weight fraction of dissolved organic matter was most reduced in concentration while substances with low molecular weight increased. The reduction in absorbance (λ = 254 nm) per DOC was most significant for substances with high molecular weight. The final concentration of DOC was highest in samples where microbial activity was suppressed.  相似文献   

Patterns of dissolved organic matter in subarctic peatlands     

T. R. Moore 《地球表面变化过程与地形》1987,12(4):387-397

Samples of water from poor to very rich fens in the Schefferville region of subarctic Quebec revealed strong spatial and temporal variations in dissolved organic carbon (DOC), ranging from 2 to 40 mg 1^?1. Concentrations of DOC tend to increase during the summer and decrease in the autumn, at most sites, which probably reflects increased plant tissue decomposition and higher rates of evapotranspiration. Principal components analysis revealed that DOC is strongly associated with Fe, NO^?₃-N and NO^?₂-N, but essentially independent of other chemical properties of the peat water, such as pH, Ca, Mg, K, P, and NH⁺₄-N. Based on observed concentrations of DOC and estimates of summer runoff (June to September), export of DOC from four peatlands ranges from 1·1 to 4·9 gCm^?2, with the lowest values for peatlands underlain by dolomite. Molecular weight fractionation of four samples revealed significant differences in the dissolved organic matter (DOM), with the largest fractions (GF/C to 10 000 nmw) being dominant in the more acid samples. The ratio of absorbance at 400 and 600 nm wavelengths (E₄:E₆) has been used as a simple indicator of differences in DOM type, ranging from 3 to 15. There is a strong seasonal pattern of increasing E₄:E₆ ratio during the summer at many sites, though this ratio is essentially independent of other chemical properties of peat waters.  相似文献   

云南临沧地区帮卖盆地含铀煤中锗矿的研究   总被引：8，自引：0，他引：8  

张淑苓  王淑英  尹金双 《铀矿地质》1987,(5)

帮卖盆地是一个不对称山间向斜盆地,其基底为海西·燕山期(γ~3_4-γ~2_5)花岗岩体。盖层为新第三纪的含煤碎屑岩。锗矿体大部分存在于N_1~2煤层中。含铀煤主要为变质程度低的褐煤,属于半暗-半亮煤、暗亮煤及亮暗煤。锗在煤中的存在形式:1.主要为腐植酸锗络合物及锗的有机化合物;2.一部分呈吸附状态;3.极少数呈类质同象。  相似文献   

Properties of humic acids as biomarkers of lake catchment management   总被引：1，自引：0，他引：1  

Joanna?CieslewiczEmail author  Slawomir?S.?Gonet 《Aquatic Sciences - Research Across Boundaries》2004,66(2):178-184

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Application of Greek lignite as an additive for controlling rheological and filtration properties of water–bentonite suspensions at high temperatures: A review     

Vassilios C. Kelessidis  Cassiani Papanicolaou  Antonios Foscolos 《International Journal of Coal Geology》2009,77(3-4):394-400

This review paper presents the results of an extensive study investigating whether addition of 3% w/w Greek lignite to 6.42% w/w water–bentonite suspensions, after being exposed to high temperatures, can prevent gelation and control filtration characteristics. Two different bentonites and eight lignites from different Greek basins have been used while a commercial lignite product has been used as standard. The lignite-free bentonite suspensions heated to 177 °C for 16 h (thermal aging) thicken considerably, increasing the yield stress and the yield point. Fluid consistency and flow behavior indices also change while no significant change is observed for plastic viscosity. Thermal aging of the suspensions results in unacceptably high fluid loss values.Addition of Greek lignite to water–bentonite suspensions, followed by thermal aging, provided the rheological stability of the suspensions by maintaining the low yield stress/point regardless of the type of bentonite. Some of the lignites performed as well as their commercial counterpart. No specific trends for rheological improvement have been identified with respect to various characteristics of lignites such as contents of humic, fulvic acids, humins and other parameters such as specific surface area and cation exchange capacity.Furthermore, addition of lignite in most cases provided very good filtration control of the water–bentonite suspensions after exposure to 177 °C, with some Greek lignites being superior to the commercial product. The same lignite parameters examined for rheological control, were also examined to determine their effect on fluid loss of these suspensions for both bentonites. The content of humic and fulvic acids of two groups of lignites showed weak inverse correlations with the fluid loss volumes for both bentonites, while all other parameters did not seem to directly correlate with the effectiveness of the lignites.  相似文献   

Sorption of Pb,Cu, Cd,and Zn by Municipal Solid Waste Composts: Metal Retention and Desorption Mechanisms     

《洁净——土壤、空气、水》2017,45(1)

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Spectroscopic Characterization of Organic Structures and Organic‐Inorganic Interactions in Paper Mill Sludge     

Claudia M. B. F. Maia  Fabio Simonelli  Antinio S. Mangrich 《洁净——土壤、空气、水》2001,28(7):372-377

The organic composition and organic‐inorganic interaction in paper mill sludge (PS) solvent extracts (hexane, ethyl acetate, acetone and ethanol) and humic fractions, humic acid (HA) and humin (HU) were studied by electron paramagnetic resonance spectroscopy (EPR), proton and carbon‐13 nuclear magnetic resonance spectroscopy (¹H NMR; ¹³C NMR), Fourier‐transformed infrared spectroscopy (FTIR), and ultraviolet‐visible spectroscopy (UV‐vis). The strategy of fractionating the PS, sequentially, with organic solvents of increasing polarity is a reliable analytical procedure for humic substance sample separation because it results in more purified fractions. FTIR, ¹H NMR and ¹³C NMR results showed that hexane extract consisted mainly of aliphatic hydrocarbon structures. Their contents in the extracts decreased as the polarity of the extracting solvent increased and the content of oxygen functional groups increased. Carboxylic and carboxylate functional groups were found in the acetone extract, and ester and ether functions were predominantly found in the ethanol extract. EPR spectra revealed some Fe³⁺ complexes with rhombic structure (g₁ = 4.3; g₂ = 9.0) in the humic fractions and in all solvent extracts, except hexane. Quasi‐octahedral Fe³⁺ complexes (g = 2.3; ΔH_pp ≤ 400 G) were found in the HU fraction and in the acetone extract. The organic free radical content in the HA fraction was higher than the non‐fractionated PS sample and HU fraction.  相似文献   

Characterisation of Fulvic Acids and Glycyrrhizic Acid by Time‐of‐Flight Secondary Ion Mass Spectrometry     

Wilfried Szymczak  Manfred Wolf  Klaus Wittmaack 《洁净——土壤、空气、水》2001,28(7):350-358

Fulvic acids of different origin, spray deposited on polished silicon after dissolution in high‐purity water without any additives, were analysed by time‐of‐flight secondary ion mass spectrometry (TOF‐SIMS) in combination with oblique 24...36 keV SF₅⁺ ion bombardment. The observed, highly reproducible mass spectra cover more than five orders of magnitude in dynamic range, without background subtraction. Apart from lines due to atomic ions and low‐mass ion fragments, the mass spectra exhibit broad maxima between m/z 200...350, mainly due to a beat‐like superposition of lines at every single mass number, up to at least m/z 400. In the negative ion spectra the beats have a spacing of m/z 14, corresponding to a CH₂‐unit. The high‐mass tails of the spectra extend well beyond m/z 5000, with similar slopes in the positive and the negative ion mass spectra. The negative spectra appear to be less affected by fragmentation products than the positive spectra. Fulvic acids (FAs) of different origin show distinctly different spectra, with mean masses ranging between m/z ≈ 450 and 580 (for a low‐mass cut‐off m/z 150). To further verify the ability of TOF‐SIMS to detect molecules and clusters with masses significantly above the maxima of the FA spectra, samples of glycyrrhizic acid (GA, as GA ammonium salt with molecular weight 840) were also analysed. Parent ions as well as multimers (GA)_n were observed as positive and negative ions, up to n = 4 (m/z 3320). The results are compared with spectra recently obtained by other mass spectrometric techniques.  相似文献