注入速率对CO_2地质储存封存潜力的影响分析

国内某著名煤炭企业计划实施每年10万吨的CO2地质储存（CCS）项目,拟选了5组地层做为目标储层。但所选封存层平均渗透率在0.15~0.6mD,平均孔隙度在2~6%,属于低渗低孔地层,如不进行人工压裂提高注入层渗透率,要实现预定存储目标尚有一些困难。笔者在研究中发现,除对目标层进行一定的水裂酸化处理提高地层渗透特性可以显著提高注入性和存储能力外,CO2注入速率的变化对地层的封存能力和注入性也有明显影响。运用TOUGH2-ECO2N软件分别模拟了无水裂及水裂情况下8种不同注入速率下这些目标存储层的压力变化及CO2封存状态比例及理论最大封存能力。模拟结果表明使用水裂酸化方法对储层进行处理后,不仅可以使注入总量达到项目要求,还可使系统理论最大储存能力提高55%;并且在灌注过程中采用变速灌注方式,可以有效控制系统压力积聚,对将来实际灌注压力控制具有重要意义。     

潮汐湿地土壤碳矿化及其对电子受体响应研究进展

潮汐湿地是一种重要的湿地类型,受周期性变化的潮汐水位和盐分等特殊因子的影响,其土壤碳矿化过程亦具独特性,综述了潮汐湿地土壤碳矿化及其对电子受体响应的最新研究进展。结果表明,潮汐湿地土壤碳矿化除有氧碳矿化外,三价铁和硫酸盐还原过程主导的厌氧碳矿化也是土壤碳矿化的重要途径;潮汐湿地类型中的红树林土壤碳矿化速率高于盐沼土壤碳矿化速率,并均以二氧化碳为土壤碳矿化的主要产物;生境的差异使不同电子受体在土壤碳矿化中的作用有所不同,并受到电子受体和电子供体数量的调节;潮汐、盐分、生物干扰等是影响潮汐湿地土壤碳矿化过程的主要因子。     

Upwelling signals in radiocarbon from early 20th-century Peruvian bay scallop (Argopecten purpuratus) shells

We quantified Δ¹⁴C, δ¹⁸O, and δ¹³C cycles along ontogeny within four bay scallop (Argopecten purpuratus) shells collected from Callao Bay, Salaverry, and Sechura Bay, Peru following the 1907–1908 non-El Niño years and the 1925–1926 El Niño. Δ¹⁴C and δ¹³C generally covary; Δ¹⁴C and δ¹⁸O vary inversely. Simultaneous decreases in Δ¹⁴C and increases in δ¹⁸O in non-El Niño shells are followed by constant Δ¹⁴C and gradually decreasing δ¹⁸O, which we interpret as evidence for discrete marine upwelling events followed by warming of the initially cold upwelled water. Upwelling changes from El Niño events are detectable with difficulty in mollusk shell Δ¹⁴C.     

房山花岗岩岩体氧氢碳的同位素研究

测定了房山花岗岩侵入体的岩石、共生矿物和气液包体的氧、氢、碳的同位素组成。共生石英-黑云母和石英-全岩的δ~(18)O数据表明,房山花岗岩侵入体保存了氧同位素平衡,氧同位素温度在450—580℃之间。大多数共生黑云母-角闪石δD值的相关性基本上符合Suzuoki-Epstein关系式,可以认为房山侵入体也保存了氢同位素平衡,推算得到的岩浆流体的δD值在-70—-30之间。气液包体中CO_2的δ(13)C为-4—-8,属于一种深源碳,可以利用地下水参加岩浆后期演化的假定来解释黑云母二长闪长岩氢、碳同位素异常     

Kinetic-simulating experiment combined with GC-IRMS analysis: application to identification and assessment of coal-derived methane from Zhongba Gas Field (Sichuan Basin, China)

The main purpose of this study is to model the δ¹³C values of methane derived from coal by combining kinetic-simulating experiment with the gas chromatography-isotope ratio mass spectrum (GC-IRMS) analysis. The stable carbon isotopic variation of methane in pyrolysates with heating temperature indicates that the assumptions for both a constant kinetic isotope effect (α) and a uniform initial isotopic composition (δ¹³C_o) are impractical for explaining the carbon isotopic fractionation during coalification. For purposes of simplification, two approaches are used in this paper to deal with the heterogeneity of terrestrial organic matter. One is that, assuming a uniform initial isotopic composition (i.e., δ¹³C_{i, o}=δ¹³C_o) for all methane-generating precursors in coal, the isotopic variation of methane is fitted by adjusting ΔE_{a, i} (E_{a¹³C, i}−E_{a¹²C, i}) for each hypothetical reaction. The other is that, assuming a constant kinetic isotope effect during the whole gas formation, that is all ΔE_{a, i} values are identical, the modeling of methane isotopic composition is achieved by changing the ¹³CH₄ generation potential of each reaction (f_{i, ¹³C}), namely, by adjusting the initial δ¹³C value (δ¹³C_{i, o}) for each methane-generating precursor. Results of the kinetic calculation shows that the two simulating methods can yield a similar result at a geological heating rate of 2 °C/My, which further demonstrates that those natural gases with methane δ¹³C value being approximately −36‰ are possibly sourced from the upper Triassic coal measure strata in the Northwestern Sichuan Basin.     

爆裂法作为快速测定流体包裹体中二氧化碳（和其它气体）含量的手段及其在勘探中的使用：以中国山东和河北省金矿为例

The acoustic decrepitation method heats a small monomineralic sample and counts pressure impulses as the inclusions burst when they develop high internal pressures. For aqueous fluids, the decrepitation temperature is correlated with the homogenisation temperature, but gas rich fluids give a distinct and characteristic low temperature decrepitation peak which can be used to recognize gas rich fluid inclusions. This information is useful in exploration for Au deposits, which are frequently associated with CO2 rich and sometimes CH4 rich fluids. This distinctive decrepitation occurs because the CO2 rich inclusion fluids expand according to the gas law and develop internal pressures high enough to burst the host mineral grain at temperatures well below their homogenisation temperatures. In contrast, aqueous fluids condense to a liquid and vapour phase during post-entrapment cooling. Upon subsequent heating their internal pressures do not increase significantly until after homogenisation to a single phase occurs and hence they do not decrepitate ＂prematurely＂ as gas rich inclusions do. This behaviour is usually regarded as an annoyance in conventional microthermometric homogenisation studies, but can readily be used as an exploration aid to find mineralisation deposited from such gas rich fluids. Decrepitation results on samples from Cowra Ck, NSW, Australia, which have also been microthermometrically measured for CO2 content, show that amounts of less than 5 mole % CO2 are easily distinguished by decrepitation and amounts as low as 1 mole % CO2 may be determinable. Examples of the use of acoustic decrepitation in the study of 6 gold mines in the Shandong and Hebei provinces of China are discussed.     

Carbon, sulfur and O2 across the Permian–Triassic boundary

A model for the carbon and sulfur cycles across the Permian–Triassic boundary has been constructed from carbon and sulfur isotopic data. Results indicate a drop in global organic matter burial, the formation of an anoxic deep ocean, and a large drop in atmospheric oxygen over the time span 270 to 240 Ma. Much of these changes were probably due to a drop in terrestrial productivity and preservation and an increase in global aridity.     

Organic geochemistry of the Vindhyan sediments: Implications for hydrocarbons

The organic geochemical methods of hydrocarbon prospecting involve the characterization of sedimentary organic matter in terms of its abundance, source and thermal maturity, which are essential prerequisites for a hydrocarbon source rock. In the present study, evaluation of organic matter in the outcrop shale samples from the Semri and Kaimur Groups of Vindhyan basin was carried out using Rock Eval pyrolysis. Also, the adsorbed low molecular weight hydrocarbons, methane, ethane, propane and butane, were investigated in the near surface soils to infer the generation of hydrocarbons in the Vindhyan basin. The Total Organic Carbon (TOC) content in shales ranges between 0.04% and 1.43%. The S₁ (thermally liberated free hydrocarbons) values range between 0.01–0.09 mgHC/gRock (milligram hydrocarbon per gram of rock sample), whereas the S₂ (hydrocarbons from cracking of kerogen) show the values between 0.01 and 0.14 mgHC/gRock. Based on the T_max (temperature at highest yield of S₂) and the hydrogen index (HI) correlations, the organic matter is characterized by Type III kerogen. The adsorbed soil gas, CH₄ (C₁), C₂H₆ (C₂), C₃H₈ (C₃) and nC₄H₁₀, (nC4), concentrations measured in the soil samples from the eastern part of Vindhyan basin (Son Valley) vary from 0 to 186 ppb, 0 to 4 ppb, 0 to 5 ppb, and 0 to 1 ppb, respectively. The stable carbon isotope values for the desorbed methane (δ¹³C₁) and ethane (δ¹³C₂) range between −45.7‰ to −25.2‰ and −35.3‰ to −20.19‰ (VPDB), respectively suggesting a thermogenic source for these hydrocarbons. High concentrations of thermogenic hydrocarbons are characteristic of areas around Sagar, Narsinghpur, Katni and Satna in the Son Valley. The light hydrocarbon concentrations (C₁–C₄) in near surface soils of the western Vindhyan basin around Chambal Valley have been reported to vary between 1–2547 ppb, 1–558 ppb, 1–181 ppb, 1–37 ppb and 1–32 ppb, respectively with high concentrations around Baran-Jhalawar-Bhanpur-Garot regions (Kumar et al., 2006). The light gaseous hydrocarbon anomalies are coincident with the wrench faults (Kota – Dholpur, Ratlam – Shivpuri, Kannod – Damoh, Son Banspur – Rewa wrench) in the Vindhyan basin, which may provide conducive pathways for the migration of the hydrocarbons towards the near surface soils.     

距今14亿年低生物量的碳同位素证据

北京十三陵和天津蓟县两剖面中距今十四亿年海相碳酸盐岩的碳同位素表明,十三陵—蓟县地区当时具有较低的δ¹³C 值(共分析了152个样品),平均占δ¹³C=-0.7‰(PDB)。这种较低的δ¹³C 值很可能具有全球性。原始的海相碳酸盐岩较低的碳同位素组或反映较低的有机碳埋藏速率。有机碳的埋藏速率与当时全球生物量的大小有着密切的关系。磷酸盐岩较低的δ¹³C 值进一步反映当时较小的全球生物量的存在。每年8.11×10⁸吨有机碳推测是距今十四亿年全球生物量的最小值。     

The effects of carbon dioxide leakage on fractures, and water quality of potable aquifers during geological sequestration of CO2

Since industrial revolution, the ＂greenhouse effect＂ is one of the most important global environmental issues. Of all the greenhouse gases, CO2 is responsible for about 64% of the enhanced ＂greenhouse effect＂, making it the target for mitigation, so reducing anthropogenic discharge of carbon dioxide attracts more and more attention. Geological sequestration of CO2 in deep saline aquifers is one of the most promising options. But because unknown fractures and faults may exist in the caprock layers which can prevent the leakage of CO2, CO2 will leak upward into upper potable aquifers, and lead to adverse impacts on the shallow potable aquifers. In order to assess the potential effect of CO2 leakage from underground storage reservoirs on fractures and water quality of potable aquifers, this study used the non-isothermal reactive geochemical transport code TOUGHREACT developed by Xu et al to establish a simplified 2-D model of CO2 underground sequestration system, which includes deep saline aquifers, caprock layers, and shallow potable aquifers, and study and analyze the changes of mineral and aqueous components. The simulation results indicated that the minerals of deep saline aquifers and fractures should be mainly composed of aluminosilicate and silicate minerals, which not only enhance the mass of CO2 sequestrated by mineral trapping, but also decrease the porosity and permeability of caprock layers and fractures to prevent and reduce CO2 leakage. The results from deep saline aquifers showed that the mass of carbon dioxide trapped by minerals and solution phases is limited, the rest remained as a supercritical phase, and so once the caprock aquifers have some unknown fractures, the free carbon dioxide phase may leak from CO2 geologic sequestration reservoirs by buoyancy.