煤岩的显微构造特征及其与瓦斯突出的关系——以南桐鱼田堡煤矿为例

煤瓦斯突出与煤岩显微结构构造密切相关。除部分显微结构构造与成煤阶段的环境等有关外,大部分都是构造变形的结果。因此,我们从构造变形类型和特点来划分煤岩显徽构造类型,既简便又利于应用。根据四川南桐鱼田堡煤矿4号及6号煤层的扫描电子显微镜研究,可将煤岩划分成5类:非构造煤、微裂隙煤、微劈理煤、碎裂构造煤和糜棱构造煤。文中详述了各类煤的特点,指出它们所代表的构造意义,并讨论了它们与瓦斯突出的关系。还特别提出糜棱构造煤的一系列塑性变形特征。得出结论:若其他条件均具备,有糜棱构造煤产出的地段,就可能是瓦斯突出最危险的部位。此外,根据观察煤瓦斯突出后的煤岩显微构造变化,提出有关瓦斯突出的过程,并探讨了煤瓦斯突出机理。在瓦斯突出过程中,已经历过塑性变形的煤岩又叠加了脆性变形,因而发生大量煤“粉尘”随突出而抛出。     

柴北缘鱼卡地区中侏罗统石门沟组含煤层段沉积有机相分析

柴达木盆地北缘鱼卡地区中侏罗统石门沟组含煤段中发育有油页岩、煤、碳质泥岩和泥岩等富有机质细粒沉积.为了研究其沉积有机相的类型及煤和油页岩形成的控制因素,本文通过岩心观察、工业分析结合有机地球化学测试分析等方法将含煤段细粒沉积物划分为了类型A(三角洲平原沉积环境)、B(三角洲前缘-浅湖沉积环境)、C1(湖沼非油页岩亚相)及C2(湖沼油页岩亚相)四种类型,其中类型C1沉积物中发育煤,类型C2中发育油页岩,且煤较油页岩具有更高的含油率、水分、挥发分以及发热量值.有机质类型特征方面,沉积有机相类型A、B及C1沉积物有机质类型均为Ⅱ2-Ⅲ型、有机质来源均以陆源和混合来源两种有机质来源为主,而类型C2中主要为Ⅱ2型,以混合有机质来源为主;类型A及C2其沉积物有机质均处于未成熟阶段,而类型B和C1中有机质均处于未成熟-低成熟阶段;有机质保存条件方面,类型A沉积物主要形成于缺氧的淡水环境,类型B主要形成于贫氧-缺氧的淡水-半咸水环境,类型C1形成于贫氧-缺氧的淡水-半咸水环境,而类型C2则主要形成于缺氧的淡水-半咸水环境.其中类型B较类型A,类型C2较类型C1,其沉积物均形成于更为还原且盐度更高的水体环境中.石门沟组含煤段是煤和油页岩的形成层位,稳定的沉积环境、丰富的湖泊有机质来源、良好的保存条件及较少的陆源碎屑的稀释共同促进了类型C2中油页岩的形成,而丰富的陆源植物供给及良好的保存条件则促进了类型C1中煤层的形成.     

论煤层的加积方式

煤层成因是煤地质学的核心。煤层是一种沉积地层,它遵循沉积学、地层学、岩石学以及矿床学的基本规律,也有其特殊性,其成因并不同于煤的成因。传统煤地质学的核心观点是煤层由泥炭沼泽演化而成,其本质就是成煤物质的垂向加积。通过对煤层垂向和侧向加积的分析对比以及大面积稳定展布的厚煤层低自然伽马多峰现象、层理与条带结构等沉积特征的研究,认为成煤物质是机械沉积的,煤层像大多数沉积岩层一样是侧向加积形成的。对于厚煤层而言,多期侧向加积产生了次生垂向加积,其形成过程不是一个简单的、连续的、线性的垂向累加过程,而是一个复杂的、不连续的、非线性的侧向叠合过程,成煤物质是不连续的、多期多源的,厚煤层中普遍存在的夹矸便是其不连续的证据,同时厚煤层是穿时的。煤层侧向加积与较深水或海相沉积共生,是一个有机连续的整体,符合瓦尔特相律和古生态学原理,符合煤层厚度、形态多变及下伏地层沉积体系多种多样,也符合成煤物质超巨量工业富集、含煤地层灰色灰黑色、煤矿床质量优良的事实。     

Occurrence and Distribution of Organic Contaminants in the Aquatic System in Berlin.Part II: Substituted Phenols in Berlin Surface Water

In a surface water screening, 30 representative surface water samples collected from rivers, canals, and lakes in Berlin were investigated for the presence of 22 substituted phenols. The phenols selected include the 11 phenols considered as “priority pollutants” by the US Environmental Protection Agency (US-EPA). Surface water samples were extracted applying solid-phase extraction with styrenedivinylbenzene adsorbent. The recoveries, determined in spiking experiments, were between 80 % and 103 %. After derivatization with N-(tert-butyldimethylsilyl)-N-methyl-trifluoroacetamide (MTBSTFA) the samples were analyzed by capillary gas chromatography-mass spectrometry (GC-MS). Phenol, cresols, 2-ethylphenol, 2-chlorophenol, 4-chloro-3-methylphenol, pentachlorophenol, 2-nitrophenol, and 4-nitrophenol were detected in the surface water samples at concentrations between 0.02 μg/L and 7.8 μg/L, respectively. The distribution of these residues in the Berlin surface waters showed that the phenolic residues, with the exception of pentachlorophenol and 2-ethylphenol, do not originate primarily from municipal sewage treatment plants discharges. Some of the phenols are formed naturally or occur as ubiquitous anthropogenic contaminants in the aquatic system.     

黑龙江密山地区晚石炭世含煤岩系沉积和构造特征

从建造和改造两个方面,系统研究了晚石炭世珍子山组的发育特征,分析了与赋煤有关的地质因素。结果表明:珍子山组含煤段沉积厚度比较稳定,含煤性较好,受后期构造破坏较轻,是较好的赋煤区。该研究为密山地区进一步找煤指出了方向。     

IMPACT OF DIABATIC PROCESSES IN AGCM ON 4-DIMENSIONAL VARIATIONAL DATA ASSIMILATION*

The impact of diabatic processes on 4-dimensional variational data assimilation (4D-Var) was studied using the 1995 version of NCEP's global spectral model with and without full physics.The adjoint was coded manually.A cost function measuring spectral errors of 6-hour forecasts to "observation" (the NCEP reanalysis data) was minimized using the L-BFGS (the limited memory quasi-Newton algorithm developed by Broyden,Fletcher,Goldfard and Shanno) for optimizing parameters and initial conditions.Minimization of the cost function constrained by an adiabatic version of the NCEP global model converged to a minimum with a significant amount of decrease in the value of the cost function.Minimization of the cost function using the diabatic model, however,failed after a few iterations due to discontinuities introduced by physical parameterizations.Examination of the convergence of the cost function in different spectral domains reveals that the large-scale flow is adjusted during the first 10 iterations,in which discontinuous diabatic parameterizations play very little role.The adjustment produced by the minimization gradually moves to relatively smaller scales between 10-20th iterations.During this transition period,discontinuities in the cost function produced by "on-off" switches in the physical parameterizations caused the cost function to stay in a shallow local minimum instead of continuously decreasing toward a deeper minimum. Next,a mixed 4D-Var scheme is tested in which large-scale flows are first adiabatically adjusted to a sufficient level,followed by a diabatic adjustment introduced after 10 to 20 iterations. The mixed 4D-Var produced a closer fit of analysis to observations,with 38% and 41% more decrease in the values of the cost function and the norm of gradient,respectively,than the standard diabatic 4D-Var,while the CPU time is reduced by 21%.The resulting optimal initial conditions improve the short-range forecast skills of 48-hour statistics.The detrimental effect of parameterization discontinuities on minimization was also reduced.     

Kinetics and Equilibrium Sorption Studies of 4-Nitrophenol on pyrolyzed and activated oil shale residue

Sorption of the organic pollutant 4-nitrophenol (4-NP) by pyrolyzed and activated Jordanian oil-shale was studied. Pyrolyzed oil shale was prepared using a fluidized bed reactor at 520 °C in the presence of nitrogen. Physical activation was carried out by treating the pyrolyzed oil shale with CO₂ at 830 °C, while chemical activation was achieved by using KOH and ZnCl₂ as impregnating agents. Batch kinetics and isotherm studies were conducted to evaluate the sorption process. Effects of contact time, initial sorbate concentration, sorbent concentration, temperature, pH and inorganic salts (NaCl and KCl) on the sorption process by the different sorbents were considered. Chemically activated oil shale, pretreated with ZnCl₂, gave the highest uptake of 4-NP. The isotherm experimental data fit reasonably well to Langmuir, Freundlich and Redlich-Paterson models. Three kinetic models, namely the Morris-Weber, Lagergren, and Pseudo-Second-Order model (PSOM), were applied to represent the experimental results for both pyrolyzed and ZnCl₂-oil shale sorbents.     

Eignung mikrobieller Biotests für gebundene Schadstoffe Suitability of Microbial Bioassays for Bound Contaminants

Toxicity of soil spiked with water soluble and insoluble contaminants was assessed with bacteria. Three bioassays were used with common soil bacteria. Water soluble fractions from the soils were estimated in microtiterplates via dehydrogenase activity of B. cereus and growth of P. putida. A new method was developed using B. cereus to include effects of soil particles with bound contaminants. As contaminants p-nitrophenol and 2-naphthol were tested in these systems. Results indicated that the concentration of the contaminants in the soil solution is determined by soil properties. Toxicity of water soluble fractions was not only a result of the toxicant's concentration but further modified by soluble components of the soils. It is not possible to assess soil pollution from toxicity of the water soluble fraction in general, because unknown factors of the soluble soil fraction can influence toxicity greatly. The newly developed contact bioassay with B. cereus showed clearly higher toxicity of 2-naphthol estimated in soil suspension than did the comparable test system with the same bacteria using water soluble fractions only. The results stress the importance of including soil particles into bioassay procedures. It was shown that also water insoluble, bound contaminants can act as toxicants. For an estimation of toxicity under conditions more relevant for the environment, the suggested test system can provide useful information to bioavailability of bound contaminants.     

Stable carbon isotope variations in northwest Europe during the last glacial–interglacial transition

Stable carbon isotope data that span part of the last glacial–interglacial transition (ca. 14-9 ka ¹⁴C BP; ca. 15–11 ka cal. BP), and which derive from organ-specific plant macrofossils recovered from two lake sediment profiles in the UK and one in Norway, are compared. The recorded temporal variations show similar trends, which, over a millennial time-scale appear to parallel the main drift in δ¹⁸O as determined for the GRIP ice-core. It is postulated that some smaller scale variations in the δ¹³C profiles may reflect the shorter term oscillations in δ¹⁸O values evident in the GRIP record, although this is less certain. Overall, however, the results suggest that stable carbon isotope measurements based on organ-specific terrestrial plant macrofossils may provide (i) a means for establishing correlations between terrestrial successions and (ii) additional paleoenvironmental information, as the apparent ‘shadowing’ of the GRIP record indicates a common forcing mechanism for both Greenland δ¹⁸O and northwest European δ¹³C variations. From the evidence available we suggest that the recorded δ¹³C variations reflect fluctuations in air temperature and/or changes in water vapour pressure in the atmosphere. © 1997 John Wiley & Sons, Ltd.     

Raman Micro-Spectroscopic Study of Sulfate Ion in the System Na2SO4 – H2O

This work aims to quantify sulfate ion concentrations in the system Na₂SO₄-H₂O using Raman micro-spectroscopy.Raman spectra of sodium sulfate solutions with known concentrations were collected at ambient temperature（293 K） and in the 500 cm^₁-4000 cm^-1 spectral region.The results indicate that the intensity of the SO₄^2- band increases with increasing concentrations of sulfate ion.A linear correlation was found between the concentration of SO₄^2-（c） and parameter I₁,which represents the ratio of the area of the SO₄^2- band to that of the O-H stretching band of water（A_s/A_w）:I₁=-0.00102+0.01538 c.Furthermore,we deconvoluted the O-H stretching band of water(2800 cm^-1-3800 cm^-1) at 3232 and 3430 cm^-1 into two sub-Gaussian bands,and then defined Raman intensity of the two sub-bands as A_Bi(3232 cm^-1) and A_B2(3430 cm^-1),defined the full width of half maximum（FWHM） of the two sub-bands as W_B1(3232 cm^-1) and W_B2(3430 cm^-1).A linear correlation between the concentration of SO₄^2-（c） and parameter I₂,which represents the ratio of Raman intensity of SO₄^2-（A_s）(in 981 cm^-1) to(A_B1+A_B2),was also established:I₂=-0.0111+0.3653 c.However,no correlations were found between concentration of SO₄^2-（c） and FWHM ratios,which includes the ratio of FWHM of SO₄^2-（W_s） to W_B1 W_B2 and W_B1+B2(the sum of W_B1 and W_B2),suggesting that FWHM is not suitable for quantitative studies of sulfate solutions with Raman spectroscopy.A comparison of Raman spectroscopic studies of mixed Na₂SO₄ and NaCI solutions with a constant SO₄^2- concentration and variable CI^- concentrations suggest that the I\ parameter is affected by CI^-,whereas the I₂ parameter was not.Therefore,even if the solution is not purely Na₂SO₄-H₂O,SO₄^2- concentrations can still be calculated from the Raman spectra if the H₂O band is deconvoluted into two sub-bands,making this method potentially applicable to analysis of natural fluid inclusions.