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。     

采空区对CO2置换开采海域天然气水合物置换效果影响的实验研究

为揭示固体开采形成的采空区对CO₂置换开采天然气水合物置换效果的影响,开展了含采空区储层与完整储层的CO₂/N₂置换开采不同天然气水合物饱和度对比实验研究。结果表明：对于水合物饱和度分别为30%和45%的试样,含采空区储层较完整储层的CH₄置换率分别提高了5.5%和9%,单位体积CO₂封存量分别提高了26.5%和39.8%。采空区的存在提高了置换介质与天然气水合物的摩尔比率,从而提供了更高的置换驱动力;且在较高水合物饱和度试样中采空区还会提高置换介质的扩散作用,导致含采空区储层的置换效果好于完整储层。因此,在固体开采后进一步进行CO₂置换开采,可以提高置换开采效率,同时有助于碳封存与地层稳定,是一种潜在的海域天然气水合物安全、绿色开采模式。     

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。     

砂岩中绿泥石含量对CO_2矿物封存影响的模拟研究

二氧化碳地质储存是实现二氧化碳减排的有效手段,砂岩储层是二氧化碳地质储存的主要储层类型之一。砂岩储层中的绿泥石溶解对二氧化碳地质储存形式和储存量有着重要的影响。依据某砂岩储层的实测资料,采用数值模拟技术,分析了绿泥石作用下CO2矿物封存机理和绿泥石含量对CO2的矿物封存量的影响。研究结果表明,绿泥石体积分数增大,溶解后可以向溶液中提供更多的Mg2+、Fe2+,有利于固碳矿物菱铁矿和铁白云石生成;绿泥石的体积分数与CO2矿物封存量有良好的正相关性,高绿泥石含量有助于砂岩储层的CO2矿物捕获。     

新疆准噶尔盆地独山子泥火山天然气地球化学特征

独山子泥火山位于新疆准噶尔盆地南缘, 地处北天山山前坳陷带的独山子背斜轴部。本文通过分析独山子泥火山喷出天然气组分及其碳同位素研究, 对天然气的来源进行了判识。3个天然气样中δ¹³C₁值均在–41‰左右, C₁/(C₂+C₃)<20, 为热成因气; δ¹³C_(C2-C1)在15‰左右, iC₄/nC₄和C₂/C₃值均较高, 说明天然气曾遭受了厌氧微生物降解作用; 其中两个喷口的天然气δ¹³C_CO2值超过+10‰, 说明天然气在受微生物降解后发生CO₂还原作用二次生成甲烷, 而另外一个喷口δ¹³C_CO2值无正异常, 未发生CO₂还原作用。不同喷口相同成因天然气在储藏或运移过程中发生不同的改造作用, 说明泥火山不同喷口对应不同的天然气运移通道或储藏条件。     

玄武岩CO2 地质封存研究进展

玄武岩CO2 地质封存相比于常规的封存技术（如驱油驱气注入封存和深部咸水层封存）,具有能促进快速碳矿化、封存效果长期且安全及封存容量巨大等明显优点。目前玄武岩CO2 封存理论方面的研究已经取得了大量进展：① 对常见主要成岩矿物的封存能力进行了排序;② 进一步了解玄武岩的矿物成分、玄武岩层内孔隙分布特征及其形成机理;③ 完善了对玄武岩CO2 封存机理、反应速率及影响因素等方面的认识;④ 查明了玄武岩在地球上的分布并评估了各种典型玄武岩的封存潜力;⑤ 发现适合于CO2 封存的场地主要包括大陆溢流型玄武岩、洋底高原玄武岩和洋中脊玄武岩等三种类型,并对目标储层选择提出了初步评价标准。本文在综述玄武岩固碳机理、玄武岩CO2 地质封存潜力及封存场地与目标储层选择的基础上,介绍了世界上已有的三个玄武岩CO2 地质封存工程示范项目：冰岛Carbfix、美国Wallula和日本Nagaoka,探讨了玄武岩CO2 地质封存存在的若干问题：① 反应速率受多种因素影响,对最终封存效果起着决定性作用;② 堵塞或压裂和保护层会影响注入封存的稳定性或可持续性;③ 封存潜力评价方法和结果不同;④ 封存场地选址和储层选择缺乏统一标准与规范;⑤ Carbfix方法的使用受限。     

二氧化碳地质封存中“对流混合”过程的研究进展

各国政府和科学家已经认识到CO2地质封存是一个长期有效的温室气体减排措施.在地质封存过程中,注入的C02的存在形式对C02地质封存工程的可行性和安全性十分重要.相较于“气体”储存机制,残余“气体”储存、溶解储存和矿物储存机制对于CO2地质封存而言是更为安全的储存形式.积累于低渗透性盖层底部的C02溶解使附近区域水溶液密度增加,从而引起“对流混合”现象.这一过程可降低储层中的超临界CO2通过垂直路径(如裂隙、断层和废弃井)向上逃逸的风险,因此增加了CO2地质封存的长期性和安全性.本文综述了CO2地质封存中“对流混合”过程的研究进展,总结归纳了该研究领域中存在的不足和问题,并对下一步研究工作提出了建议,以期为CO2地质封存中“对流混合”过程的研究在中国的深入开展提供参考.     

华北平原CO2地下埋存潜力研究

以CO<,2>地质埋存的观点开展华北平原CO<,2>埋存地质学研究,通过对主要地质要素的分析,阐述冀中坳陷的地质背景和构造演化,提出在华北平原具有3层区域性的CO<,2>封盖一储存结构:即顶层馆陶组-明化镇组组合,中层古近系多次湖盆演化形成的储盖组合以及底层古潜山碳酸盐岩储层,并且对它们的岩石性质、圈闭类型与水文地质特...     

温室气体CO2与钠长石相互作用实验研究

为寻求减缓全球变暖的途径,利用高压釜,开展不同温度下(75、100、125、150和175℃)CO₂与钠长石的水热实验研究,以探讨CO₂在长石砂岩中地质封存的可能性。结果表明,随着温度的升高,钠长石溶蚀强度逐渐增强,在150℃左右开始有菱镁矿、菱铁矿等碳酸盐矿物生成,175℃新矿物生成量增加,这表明CO₂能够以碳酸盐矿物的形式在含钠长石的长石砂岩中以矿物的形式被“固定”,其被“固定”的温度在150℃左右。     

CO2气综合识别技术及应用

CO₂气藏由于其物理、化学性质的特殊性,CO₂气勘探与烃类气既有相同又有区别,综合应用多种资料和多种技术方法是识别CO₂气(层)藏的有效手段。利用区域地质分析、地球物理和地球化学勘探方法综合评价非烃气的分布,提出钻探目标,通过非烃色谱测量法和红外线CO₂气体浓度测量法实现CO₂气层钻井现场动态检测,利用气体色谱检测相关录井参数资料、核测井密度中子孔隙度差值综合解释CO₂气层,有效地识别CO₂气。主要介绍CO₂气藏综合勘探技术的关键的新技术方法,如地球化学方法、录井和测井综合识别的关键技术方法等。     

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.     

The Effects of Small Amounts of H2O, CO2 and Na2O on the Partial Melting of Spinel Lherzolite in the System CaO-MgO-Al2O3-SiO2 {+/-} H2O {+/-} CO2 {+/-} Na2O at 1{middle dot}1 GPa

The effects of small amounts of H₂O (<4 wt % in the melt)on the multiply saturated partial melting of spinel lherzolitein the system CaO–MgO–Al₂O₃–SiO₂ ±Na₂O ± CO₂ have been determined at 1·1 GPa inthe piston-cylinder apparatus. Electron microprobe analysisand Fourier transform infrared spectroscopy were used to analysethe experimental products. The effects of H₂O are to decreasethe melting temperature by 45°C per wt % H₂O in the melt,to increase the Al₂O₃ of the melts, decrease MgO and CaO, andleave SiO₂ approximately constant, with melts changing fromolivine- to quartz-normative. The effects of CO₂ are insignificantat zero H₂O, but become noticeable as H₂O increases, tendingto counteract the H₂O. The interaction between H₂O and CO₂ causesthe solubility of CO₂ at vapour saturation to increase withincreasing H₂O, for small amounts of H₂O. Neglect of the influenceof CO₂ in some previous studies on the hydrous partial meltingof natural peridotite may explain apparent inconsistencies betweenthe results. The effect of small amounts of H₂O on multiplysaturated melt compositions at 1·1 GPa is similar tothat of K₂O, i.e. increasing H₂O or K₂O leads to quartz-normativecompositions, but increasing Na₂O produces an almost oppositetrend, towards nepheline-normative compositions. KEY WORDS: H₂O; CO₂; FTIR; hydrous partial melting; mantle melting; spinel lherzolite; system CaO–MgO–Al₂O₃–SiO₂ ± H₂O ± CO₂ ± Na₂O     

Continuous Gradations among Primary Carbonatitic, Kimberlitic, Melilititic, Basaltic, Picritic, and Komatiitic Melts in Equilibrium with Garnet Lherzolite at 3-8 GPa

Multianvil melting experiments in the system CaO–MgO–Al₂O₃–SiO₂–CO₂(CMAS–CO₂) at 3–8 GPa, 1340–1800°C, involvingthe garnet lherzolite phase assemblage in equilibrium with CO₂-bearingmelts, yield continuous gradations in melt composition betweencarbonatite, kimberlite, melilitite, komatiite, picrite, andbasalt melts. The phase relations encompass a divariant surfacein P–T space. Comparison of the carbonatitic melts producedat the low-temperature side of this surface with naturally occurringcarbonatites indicates that natural magnesiocarbonatites couldbe generated over a wide range of pressures >2·5 GPa.Melts analogous to kimberlites form at higher temperatures alongthe divariant surface, which suggests that kimberlite genesisrequires more elevated geotherms. However, the amount of waterfound in some kimberlites has the potential to lower temperaturesfor the generation of kimberlitic melts by up to 150°C,provided no hydrous phases are present. Compositions resemblinggroup IB and IA kimberlites are produced at pressures around5–6 GPa and 10 GPa, respectively, whereas the compositionsof some other kimberlites suggest generation at higher pressuresstill. At pressures <4 GPa, an elevated geotherm producesmelilitite-like melt in the CMAS–CO₂ system rather thankimberlite. Even when a relatively CO₂-rich mantle compositioncontaining 0·15 wt % CO₂ is assumed, kimberlites andmelilitites are produced by <1% melting and carbonatitesare generated by even smaller degrees of melting of <0·5%. KEY WORDS: carbonatite; CO₂; kimberlite; melilitite; melt generation     

鄂尔多斯盆地伊金霍洛旗附近二叠系石千峰组岩石学、地球化学特征及其固碳能力分析

鄂尔多斯盆地是我国CO2地下埋藏的潜在目标区,位于伊金霍洛旗附近的中神监X井与CO2地下注入井中神注1井相邻,两者钻遇地层系统和岩石组合一致。为对示范区储层的固碳潜力和泥岩改造状况做出预测,为CO2地质储存的数值模拟研究提供基础地质信息和相关数据,通过偏光显微镜、扫描电镜、X射线衍射、X射线荧光等多种技术手段,开展了中神监X井石千峰组的岩石学和地球化学特征研究。结果表明石千峰组的砂岩岩石类型主要为长石岩屑砂岩和岩屑长石砂岩;泥岩主要由石英、粘土矿物和长石组成,其中,粘土矿物主要为伊利石,其次为蒙皂石、高岭石和绿泥石。预测在CO2注入后的流体-砂岩长期相互作用过程中,石千峰组砂岩可以通过形成片钠铝石、方解石、铁白云石和菱铁矿等固碳矿物,形成对CO2泄露而言的矿物圈闭,进而实现CO2的长期和安全封存;红色泥岩夹层将发生金属离子活化,导致泥岩褪色。     

全国二氧化碳地质储存适宜性评价编图技术方法研究

将全国CO2地质储存潜力与适宜性评价工作划分为5个阶段,依次为区域级预测潜力(E级)评价、盆地级推定潜力(D级)评价、目标区级控制潜力(C级)评价、场地级基础储存量(B级)评价和灌注级工程储存量(A级)评价阶段.第一阶段编制的成果图件主要为全国1∶500万CO2地质储存成果图系;第二、三阶段主要编制沉积盆地CO2地质储存成果图集;第四、五阶段主要编制CO2地质储存示范工程成果图册.提出中国CO2地质储存潜力与适宜性评价和编图是一项有步骤、分阶段逐步完成的工程,评价及编图方法有待通过潜力与适宜性评价和编图的实践不断完善.     

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.     

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.     

Experimental Investigation and Optimization of Thermodynamic Properties and Phase Diagrams in the Systems CaO-SiO2, MgO-SiO2, CaMgSi2O6-SiO2 and CaMgSi2O6-Mg2SiO4 to 1{middle dot}0 GPa

Using experimental results at 1·0 GPa for the systemsCaO–SiO₂, MgO–SiO₂, CaMgSi₂O₆–SiO₂ and CaMgSi₂O₆–Mg₂SiO₄,and all the currently available phase equilibria and thermodynamicdata at 1 bar, we have optimized the thermodynamic propertiesof the liquid phase at 1·0 GPa. The new optimized thermodynamicparameters indicate that pressure has little effect on the topologyof the CaO–SiO₂, CaMgSi₂O₆–SiO₂, and CaMgSi₂O₆–Mg₂SiO₄systems but a pronounced one on the MgO–SiO₂ binary. Themost striking change concerns passage of the MgSiO₃ phase fromperitectic melting at 1 bar to eutectic melting at 1·0GPa. This transition is estimated to occur at 0·41 GPa.For the CaMgSi₂O₆–SiO₂ and CaMgSi₂O₆–Mg₂SiO₄ pseudo-binaries,the size of the field clinopyroxene + liquid increases withincreasing pressure. This change is related to the shift ofthe piercing points clinopyroxene + silica + liquid (from 0·375mol fraction SiO₂ at 1 bar to 0·414 at 1·0 GPa)and clinopyroxene + olivine + liquid (from 0·191 molfraction SiO₂ at 1 bar to 0·331 at 1·0 GPa) thatbound the clinopyroxene + liquid field in the CaMgSi₂O₆·SiO₂and CaMgSi₂O₆·Mg₂SiO₄ pseudo-binaries, respectively. KEY WORDS: CaO–SiO₂; CaMgSi₂O₆–Mg₂SiO₄; CaMgSi₂O₆–SiO₂; experiments; MgO–SiO₂     

中国二氧化碳地质储存潜力评价与示范工程

2010—2012年,中国地质调查局水文地质环境地质调查中心承担完成的“全国二氧化碳地质储存潜力评价与示范工程计划项目”,全面建立了我国二氧化碳地质储存潜力与适宜性评价指标体系与评价技术方法,评价了主要沉积盆地的二氧化碳地质储存潜力与适宜性,完成了全国1∶500万评价图系和主要盆地评价图集编制,圈定出一批二氧化碳地质储存目标靶区;构建了深部咸水层二氧化碳地质储存工程选址、场地勘查与评价技术方法;与神华集团合作,在内蒙古鄂尔多斯市伊金霍洛旗成功实施了我国首个深部咸水层二氧化碳地质储存示范工程,基本形成了我国二氧化碳地质储存基本理论和技术方法体系。     

The Role of Advective Fluid Flow and Diffusion during Localized, Solid-State Dehydration: Sondrum Stenhuggeriet, Halmstad, SW Sweden

A localized dehydration zone, Söndrum stone quarry, Halmstad,SW Sweden, consists of a central, 1 m wide granitic pegmatoiddyke, on either side of which extends a 2·5–3 mwide dehydration zone (650–700°C; 800 MPa; orthopyroxene–clinopyroxene–biotite–amphibole–garnet)overprinting a local migmatized granitic gneiss (amphibole–biotite–garnet).Whole-rock chemistry indicates that dehydration of the graniticgneiss was predominantly isochemical. Exceptions include [Y+ heavy rare earth elements (HREE)], Ba, Sr, and F, which aremarkedly depleted throughout the dehydration zone. Systematictrends in the silicate and fluorapatite mineral chemistry acrossthe dehydration zone include depletion in Fe, (Y + HREE), Na,K, F, and Cl, and enrichment in Mg, Mn, Ca, and Ti. Fluid inclusionchemistry is similar in all three zones and indicates the presenceof a fluid containing CO₂, NaCl, and H₂O components. Water activitiesin the dehydration zone average 0·36, or X_H2O = 0·25.All lines of evidence suggest that the formation of the dehydrationzone was due to advective transport of a CO₂-rich fluid witha minor NaCl brine component originating from a tectonic fracture.Fluid infiltration resulted in the localized partial breakdownof biotite and amphiboles to pyroxenes releasing Ti and Ca,which were partitioned into the remaining biotite and amphibole,as well as uniform depletion in (Y + HREE), Ba, Sr, Cl, andF. At some later stage, H₂O-rich fluids (H₂O activity >0·8)gave rise to localized partial melting and the probable injectionof a granitic melt into the tectonic fracture, which resultedin the biotite and amphibole recording a diffusion profile forF across the dehydration zone into the granitic gneiss as wellas a diffusion profile in Fe, Mn, and Mg for all Fe–Mgsilicate minerals within 100 cm of the pegmatoid dyke. KEY WORDS: charnockite; fluids; CO₂; brines; localized dehydration; Söndrum