砂岩中片钠铝石的特征及其稳定性研究

片钠铝石是一种斜方晶系、含水、钠和铝的碳酸盐矿物,砂岩中的片钠铝石是最晚形成的自生矿物之一,一般以放射状、束状、毛发状、板状等分布于砂岩的孔隙中或交代长石和岩屑等。片钠铝石是在高CO₂分压,温度在25~100℃,碱性—弱酸性流体条件下形成的。片钠铝石的溶解实验表明,地层条件下片钠铝石发生溶解的温度区间为100~150℃,且反应后有碳酸盐及其他矿物生成。片钠铝石在100℃时的稳定和新碳酸盐矿物的生成表明,地层条件下片钠铝石能够稳定存在,能够实现CO₂在地下的永久贮存。     

沉积岩中无机CO2热模拟实验研究

结合三水盆地的地质特点，分析了无机CO₂热模拟实验研究的可能性，进行了不同条件下的模拟试验和相关的分析测试，提出了无机CO₂生成量和转化率的概念和计算方法。从实验结果来看：含有一定量碳酸盐矿物的沉积岩，在一定温度下可转化形成相当数量的无机CO₂，无机CO₂转化率越高，岩石中碳酸盐矿物越容易转化生成无机CO₂；相同热成熟度条件下，Ⅱ型干酪根生成有机CO₂的量较Ⅲ型的少；CO₂中碳同位素与CO₂的成因密切相关，随有机质热成熟度的增加，同种类型有机质生成的有机CO₂相对富集¹³C；无机CO₂较有机CO₂的碳同位素明显富集¹³C，随水介质的pH值降低，无机CO₂气含量、模拟温度及时间的增加，无机CO₂相对富集¹³C。实验研究结果为CO₂成因研究及其资源评价提供了实验依据。     

CO_2流体与储层砂岩相互作用机理实验

储存于地下岩层中的CO2与矿物发生化学反应导致次生碳酸盐矿物的沉淀,CO2将以碳酸盐矿物的形式长时间地固结在储层岩石中,从而有效减少CO2向大气中的排放。通过对不同温度下CO2-H2O-砂岩相互作用机理的研究,以及反应后样品的扫描电镜观察、质量损失量和剩余反应液中总矿化度变化的分析发现:砂岩样品的溶蚀程度随温度的升高而逐渐增强;100℃和175℃时样品表面分别有方解石和白云石生成,250℃时新生成的矿物因温度过高而溶解。这表明CO2能够以碳酸盐矿物的形式固定在矿物中,175℃为本实验所证明较适合的贮存温度。     

白云鄂博超大型稀土-铌-铁矿床成矿过程中的流体不混溶作用

白云鄂博超大型REE-Nb-Fe矿床赋存在白云岩内，矿体由磁铁矿、稀土氟碳酸盐、萤石、霓石、角闪石、方解石和重晶石等矿物组成。在白云鄂博矿床矿石和脉石矿物中赋存有两/三相富CO₂、三相高盐卤水和两相水溶液包裹体3大类型。显微测温表明富CO₂包裹体内还有近于纯的CO₂，成矿流体为H₂O-CO₂-NaCl-（F-REE）体系。高盐卤水包裹体和富CO₂包裹体共生且具有近似的完全均一温度，表明初始热液发生了流体不混溶作用。流体包裹体中出现稀土子矿物，表明初始成矿流体含有很高的稀土元素，这也许是形成白云鄂博超大型稀土矿床的原因。     

CO2流体-长石相互作用实验研究

不同温度下(100、200、300℃)CO2流体与富钾长石和斜长石的水热实验表明:随着温度的升高,长石的溶蚀强度逐渐加大,且钠长石的溶蚀程度强于钾长石。在CO2流体与富钾长石及斜长石反应后,200℃和300℃时样品表面均有球粒状、棒状及花状的水铝矿生成,且200℃时样品表面有菱铁矿生成;在CO2流体与斜长石反应后,300℃时样品表面有球形的氧化亚铁析出。这表明CO2能够以碳酸盐的形式在矿物中"固定",其被"固定"的上限温度为200℃左右。     

辽宁弓长岭铁矿床二矿区流体包裹体研究

弓长岭铁矿床二矿区富铁矿体在空间上与由石榴子石、角闪石、绿泥石等矿物组成的交代岩关系密切,显示与热液活动相关。根据交代岩中矿物共生组合、交代岩与矿体的穿插交代关系等特征,将弓长岭铁矿床二矿区富矿成矿过程分为早期热液交代阶段、晚期热液交代阶段和石英脉阶段。对这3个阶段石英中的流体包裹体进行了岩相学、显微测温和激光拉曼光谱分析。结果表明,不同测定对象中的流体包裹体类型相似,主要有富液相、富气相及含子矿物多相包裹体等类型。但它们的均一温度和盐度有明显差别,早期热液交代阶段石英中的包裹体均一温度主要集中于340~398℃,盐度主要集中于0.88%~6.3%和33.5%~40.6%两个区间,成矿流体以富CO₂的CO₂-CH₄-H₂O的中低盐度、中高温热液流体为主,并混有含石盐子矿物的高盐度、中高温热液流体,有大量磁铁矿富矿形成;晚期热液交代阶段石英中的包裹体均一温度主要集中于230~280℃,盐度主要集中于0.88%~4.96%,该阶段成矿流体为含CO₂的CO₂-H₂O±CH₄的中低温、低盐度热液流体,是富矿的较重要成矿阶段;石英脉阶段石英中的包裹体均一温度主要集中于150~180℃,盐度主要集中于1.06%~2.07%,该阶段流体为含CO₂-H₂O的低盐度、低温的热液流体,与富矿的形成关系不大。     

含片钠铝石砂岩与地层水相互作用实验

不同温度(100℃、150℃和200℃)地层水对含片钠铝石砂岩的改造作用研究显示,随着温度升高,砂岩的溶解程度逐渐增强,样品中片钠铝石的稳定性逐渐减弱。在片钠铝石溶解的同时,200℃时样品表面有高钠长石和绿泥石生成,且通过X-射线衍射分析发现,在150℃和200℃时有某种未知的碳酸盐矿物生成,生成量随温度升高而增大。100℃时片钠铝石的微弱溶解及150℃和200℃时碳酸盐矿物的生成表明,在地层条件下以片钠铝石等碳酸盐矿物形式捕获的CO2能够稳定存在。     

小秦岭东桐峪金矿床的流体包裹体研究

东桐峪金矿床位于小秦岭金矿田的中西部,其含金石英脉受韧性剪切构造带的控制。该矿床的构造-成矿过程可划分为4个阶段:Ⅰ黄铁矿-乳白色石英脉阶段;Ⅱ灰白色石英-黄铁矿阶段;Ⅲ石英-多金属硫化物阶段;Ⅳ石英-碳酸盐阶段。相对于小秦岭地区的其他金矿床,东桐峪金矿床的流体包裹体研究资料相对缺乏。文章表明,该矿床内的流体包裹体类型主要为CO₂-H₂O包裹体和水溶液包裹体,见少量纯液相CO₂包裹体。显微测温表明,Ⅰ阶段的构造-成矿流体以中温、富CO₂等挥发分为特征,包裹体均一温度为221~392℃,盐度w(NaCl_eq)为5.5%~7.9%,密度为0.84~0.93 g/cm³;Ⅱ阶段和Ⅲ阶段以CO₂-H₂O±CH₄流体为主,包裹体均一温度为205~350℃(Ⅱ阶段)和224~271℃(Ⅲ阶段),盐度w(NaCl_eq)集中于5.1%~7.1%,密度为0.83~0.96 g/cm³;Ⅳ阶段的流体演化为中-低温、低盐度的盐水溶液体系,包裹体均一温度为175~185℃。文章对该矿床各成矿阶段的压力进行了估算,Ⅰ、Ⅱ、Ⅲ阶段的流体最小捕获压力分别为123~160 MPa、160~170 MPa、170 MPa左右。     

西秦岭铧厂沟金矿床流体包裹体特征研究及矿床成因

铧厂沟金矿位于西秦岭勉略缝合带南侧,其产出受韧脆性剪切带控制,赋矿围岩为泥盆系细碧岩、凝灰质绢云千枚岩和灰岩。根据脉体穿切关系和矿物交代关系,可以将铧厂沟金矿分为早、中、晚3个成矿阶段。在铧厂沟金矿的石英中发育了CO₂-H₂O型、纯CO₂型、H₂O溶液型和含子矿物型四种类型流体包裹体。早期石英中原生包裹体主要是CO₂-H₂O型和纯CO₂型,其成分为CO₂+H₂O±N₂±CH₄±H₂S,均一温度集中在320~360℃,盐度为0.43%~5.14% NaCleqv;中阶段为主成矿阶段,该阶段石英中包含了所有四种类型的包裹体,其中H₂O溶液型包裹体占了大多数,CO₂-H₂O和水溶液包裹体均一温度集中在240~320℃,盐度为0.43%~11.19% NaCleqv;晚阶段石英仅发育水溶液型包裹体,具有较低的均一温度(118~228℃)和盐度(0.18%~6.59% NaCleqv)。根据CO₂-H₂O型包裹体计算主成矿阶段压力为70~195MPa,成矿深度为5~7km。总体而言,铧厂沟金矿的初始流体具有中高温、富CO₂、低盐度的变质流体特征,晚成矿阶段流体演化为低温、低盐度水溶液流体,流体的不混溶导致了主成矿期的矿质的大量沉淀,铧厂金矿为中浅成的造山型矿床。     

准噶尔北部希勒库都克斑岩钼铜矿床地质与成矿流体

希勒库都克斑岩铜钼矿床铜钼矿化与安山玢岩脉、英安玢岩脉有关,蚀变有钾长石化、绢云母化、绿帘石化等,向外发育绿泥石化、深部发育夕卡岩型蚀变。浅部以钼矿化为主,向深部铜钼矿化并存。与典型的斑岩型矿床相比,其石英中流体包裹体少而小,气体包裹体少,含CO₂包裹体及含子矿物包裹体发育,子矿物以NaCl为主,基本不出现KCl子矿物。钼富集处出现了富CO₂流体的沸腾,铜富集处出现了成群分布的含大子矿物包裹体,沸腾消失。钼的成矿主要与富CO₂成矿流体沸腾及斑岩型蚀变和夕卡岩蚀变有关,钼主要源于地壳,成矿温度为280~530℃,集中在300~400℃左右。铜主要与直接从深源基性岩浆出溶的高盐度流体及夕卡岩型蚀变有关,铜主要源于上地幔,主要成矿温度低于350℃。晚期流体的成矿温度为180~300℃左右。希勒库都克矿床成矿流体特征反映了壳源与幔源流体混合、岩浆热液与天水混合的特征。     

Interpretation of carbon dioxide diffusion behavior in coals

Storage of carbon dioxide in geological formations is for many countries one of the options to reduce greenhouse gas emissions and thus to satisfy the Kyoto agreements. The CO₂ storage in unminable coal seams has the advantage that it stores CO₂ emissions from industrial processes and can be used to enhance coalbed methane recovery (CO₂-ECBM). For this purpose, the storage capacity of coal is an important reservoir parameter. While the amount of CO₂ sorption data on various natural coals has increased in recent years, only few measurements have been performed to estimate the rate of CO₂ sorption under reservoir conditions. An understanding of gas transport is crucial for processes associated with CO₂ injection, storage and enhanced coalbed methane (ECBM) production.A volumetric experimental set-up has been used to determine the rate of sorption of carbon dioxide in coal particles at various pressures and various grain size fractions. The pressure history during each pressure step was measured. The measurements are interpreted in terms of temperature relaxation and transport/sorption processes within the coal particles. The characteristic times of sorption increase with increasing pressure. No clear dependence of the characteristic time with respect to the particle size was found. At low pressures (below 1 MPa) fast gas diffusion is the prevailing mechanism for sorption, whereas at higher pressures, the slow diffusion process controls the gas uptake by the coal.     

Quick-look assessments to identify optimal CO2 EOR storage sites

A newly developed, multistage quick-look methodology allows for the efficient screening of an unmanageably large number of reservoirs to generate a workable set of sites that closely match the requirements for optimal CO₂ enhanced oil recovery (EOR) storage. The objective of the study is to quickly identify miscible CO₂ EOR candidates in areas that contain thousands of reservoirs and to estimate additional oil recovery and sequestration capacities of selected top options through dimensionless modeling and reservoir characterization. Quick-look assessments indicate that the CO₂ EOR resource potential along the US Gulf Coast is 4.7 billion barrels, and CO₂ sequestration capacity is 2.6 billion metric tons. In the first stage, oil reservoirs are screened and ranked in terms of technical and practical feasibility for miscible CO₂ EOR. The second stage provides quick estimates of CO₂ EOR potential and sequestration capacities. In the third stage, a dimensionless group model is applied to a selected set of sites to improve the estimates of oil recovery and storage potential using appropriate inputs for rock and fluid properties, disregarding reservoir architecture and sweep design. The fourth stage validates and refines the results by simulating flow in a model that describes the internal architecture and fluid distribution in the reservoir. The stated approach both saves time and allows more resources to be applied to the best candidate sites.     

水射流破碎联合CO2置换开采天然气水合物新工艺及实验研究

本文对目前开采天然气水合物的5种方法进行了归纳总结,重点分析了CO₂置换开采以及固体开采法,并通过分析这2种开采方法的优劣势,提出了水射流冲蚀、破碎海洋天然气水合物储层联合CO₂置换开采天然气水合物的新思路。水射流冲蚀、破坏水合物储层后形成的采空区能为CO₂提供更好的储藏空间并提高其与储层的作用面积,提高置换效率;封存的CO₂水合物也可以提高水合物储层的稳定性,具有良好的互补效应。实验结果表明,在整个置换过程中,含采空区储层CH₄置换率为24.3%,CO₂封存率为22.1%;完整储层CH₄置换率为15.3%,CO₂封存率为20.9%,置换率提升约59%,封存率提升约5.7%。采空区的作用主要体现在提升水合物置换介质的注入量上。     

四川盆地理论CO_2地质利用与封存潜力评估

结合CO_2地质利用与封存技术机理,在国际权威潜力评估公式的基础上,系统地提出了适合中国地质背景的次盆地尺度CO_2封存潜力评估方法及关键参数取值。同时,以四川盆地为例,依次开展了枯竭油田地质封存与CO_2强化石油开采、枯竭气田与CO_2强化采气、不可采煤层地质封存与CO_2驱替煤层气,以及咸水层地质封存技术的CO_2地质封存潜力。结果表明,四川盆地利用深部咸水层与枯竭天然气田CO_2地质封存潜力最大,期望值分别达154.20×10~8t和53.73×10~8t。其中,枯竭天然气田因成藏条件好、勘探程度高、基础建设完善,为四川盆地及其周边利用枯竭气田CO_2地质封存技术实现低碳减排提供了早期示范机会。CO_2地质利用与封存潜力评估方法,对进一步开展全国次盆地尺度理论封存潜力评估与工程规划具有重要意义。     

Experimental identification of CO2–water–rock interactions caused by sequestration of CO2 in Westphalian and Buntsandstein sandstones of the Campine Basin (NE-Belgium)

Geological sequestration of CO₂ is one of the options studied to reduce greenhouse gas emissions. Although the feasibility of this concept is proven, apart from literature data on modelling still little is known about the CO₂–water–rock interactions induced by CO₂-injection.To evaluate the effect of CO₂–water–rock interactions on three sandstone aquifers in NE-Belgium an experimental setup was built. Eighteen experiments were performed in which sandstones were exposed to supercritical CO₂. CO₂–water–rock interactions were deduced from the evolution of aqueous concentrations of 25 species and a thorough characterisation of the sandstones before and after treatment. The results show that dissolution of ankerite/dolomite and Al-silicates could enhance porosity/permeability. The observed precipitation of end-member carbonates could increase storage capacity if it exceeds carbonate dissolution. Precipitation of the latter and of K-rich clays as observed, however, can hamper the injection.     

Geologic factors controlling CO2 storage capacity and permanence: case studies based on experience with heterogeneity in oil and gas reservoirs applied to CO2 storage

A variety of structural and stratigraphic factors control geological heterogeneity, inferred to influence both sequestration capacity and effectiveness, as well as seal capacity. Structural heterogeneity factors include faults, folds, and fracture intensity. Stratigraphic heterogeneity is primarily controlled by the geometry of depositional facies and sandbody continuity, which controls permeability structure. The permeability structure, in turn, has implications for CO₂ injectivity and near-term migration pathways, whereas the long-term sequestration capacity can be inferred from the production history. Examples of Gulf Coast oil and gas reservoirs with differing styles of stratigraphic heterogeneity demonstrate the impact of facies variability on fluid flow and CO₂ sequestration potential. Beach and barrier-island deposits in West Ranch field in southeast Texas are homogeneous and continuous. In contrast, Seeligson and Stratton fields in south Texas, examples of major heterogeneity in fluvial systems, are composed of discontinuous, channel-fill sandstones confined to narrow, sinuous belts. These heterogeneous deposits contain limited compartments for potential CO₂ storage, although CO₂ sequestration effectiveness may be enhanced by the high number of intraformational shale beds. These field examples demonstrate that areas for CO₂ storage can be optimized by assessing sites for enhanced oil and gas recovery in mature hydrocarbon provinces.     

二氧化碳羽流地热系统的碳封存经济分析

【研究目的】 二氧化碳羽流地热系统（CPGS）在取热的同时可实现CO₂地质封存，在碳达峰与碳中和背景下，CPGS碳封存的经济性是众多学者关注的要点。【研究方法】 以松辽盆地泉头组为例，采用数值模拟方法对比分析了注入压力、井间距与回注温度对热提取率的影响，在供暖情景下，计算了CPGS供暖效益与碳封存成本，并与常规水热型地热系统供暖效益进行了对比。【研究结果】 受携热介质转变与热突破影响，CPGS开采井温度呈现“降低-稳定-降低”的趋势，其中井间距对开采井温降影响显著，井间距越小开采井温降越明显；热提取率与回注压力呈现正相关性，与回注温度呈现负相关性，井间距对热提取率影响不显著；CPGS与常规水热型地热系统相比，采热量呈现“高-低-高”三个阶段，其中回注压力越小、回注温度与储层温度越接近，实现CPGS较水介质多采热能所需的时间越短。【结论】 仅考虑CO₂价格与取热效益，供暖收益抵消部分碳封存成本后，井间距对CO₂封存单位成本影响最为显著，井间距越小，CO₂封存单位成本降低越迅速，在注采井间距300 m条件下，持续开采30 a后CO₂封存单位成本可降至160元/t。     

The rise of trees and their effects on Paleozoic atmospheric CO2 and O2

The rise of large vascular plants during the mid-Paleozoic brought about a major increase in the rates of weathering of silicate minerals that induced a drop in the level of atmospheric CO₂ and contributed, via the atmospheric greenhouse effect, to global cooling and the initiation of the most long lived and a really extensive glaciation of the past 550 million years. Sedimentary burial of the microbiologically resistant remains of the plants resulted during the Permo-Carboniferous in both further lowering of CO₂ and in elevation of atmospheric O₂. Evidence of changes in CO₂ and O₂ are provided by mathematical models, studies of paleosols, fossil plants, fossil insects, and the effects of modern plants on silicate weathering, and by laboratory studies of the effects of changes in O₂ on plants and insects. To cite this article: R.A. Berner, C. R. Geoscience 335 (2003).     

低渗透油藏二氧化碳混相驱注采方式研究——以克拉玛依油田X区克下组低渗透油藏为例

[研究目的]克拉玛依油田X区克下组低渗透油藏存在物性差、水驱开发采收率低等问题,影响了油田的可持续发展.CO2是全球变暖的主要成分,世界各国都在想方设法减少CO2的排放量,本文试图利用CO2驱油气方式提高该油藏的采收率,变害为利.[研究方法]文章选取研究区60余口取心井目标层位岩心样品,开展扫描电镜及压汞测试分析等研究...     

Hydrometallurgical processing and recovery of molybdenum trioxide from spent catalyst

Hydrometallurgical processing of spent hydrodesulphurisation (HDS) catalyst for the recovery of molybdenum using sodium carbonate and hydrogen peroxide mixtures was investigated. The results indicated that the recovery of molybdenum was largely dependent on the concentrations of Na₂CO₃ and H₂O₂ in the reaction medium, which controls the acidity of the leach liquor and carry over of impurities such as Al, Ni, P, Si and V. Leaching process was exothermic and leaching efficiency of molybdenum decreased with increasing solid to liquid ratio. Large scale leaching of spent catalyst, under optimum conditions: 20% pulp density, 85 g/L Na₂CO₃, 10 vol.% H₂O₂ and 1 h reaction, resulted a leaching efficiency of 84% Mo. The obtained leach liquor contained (g/L): Mo — 22.0, Ni — 0.015 and Al — 0.82, P — 1.1, Si — 0.094 and minor quantities of V — 8 mg/L, As and Co — < 1 mg/L. Recovery of Mo from leach solution as MoO₃ of 97.30% purity was achieved by ammonium molybdate precipitation method.