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1.
The systematic sampling of the chemical composition of the groundwater from five karst springs (including an overflow spring) and one outflowing borehole have permitted to determine distinctive chemical changes in the waters that reflect the geochemical processes occurring in a carbonate aquifer system from southern Spain. The analysis of the dissolution parameters revealed that geochemical evolution of the karst waters basically depends on the availability of the minerals forming aquifer rocks and the residence time within the aquifers. In the three proposed scenarios in the aquifers, which include the preferential flow routines, the more important geochemical processes taking place during the groundwater flow from the recharge to the discharge zones are: CO2 dissolution and exsolution (outgassing), calcite net dissolution, calcite and dolomite sequential dissolution, gypsum/anhydrite and halite dissolution, de-dolomitization and calcite precipitation. A detailed analysis of the hydrochemical data set, saturation indices of the minerals and partial pressure of CO2 in the waters joined to the application of geochemical modelling methods allowed the elaboration of a hydrogeochemical model of the studied aquifers. The developed approach contributes to a better understanding of the karstification processes and the hydrogeological functioning of carbonate aquifers, the latter being a crucial aspect for the suitable management of the water resources.  相似文献   

2.
《Applied Geochemistry》2004,19(6):917-936
Carbon dioxide disposal into deep aquifers is a potential means whereby atmospheric emissions of greenhouse gases may be reduced. However, our knowledge of the geohydrology, geochemistry, geophysics, and geomechanics of CO2 disposal must be refined if this technology is to be implemented safely, efficiently, and predictably. As a prelude to a fully coupled treatment of physical and chemical effects of CO2 injection, the authors have analyzed the impact of CO2 immobilization through carbonate mineral precipitation. Batch reaction modeling of the geochemical evolution of 3 different aquifer mineral compositions in the presence of CO2 at high pressure were performed. The modeling considered the following important factors affecting CO2 sequestration: (1) the kinetics of chemical interactions between the host rock minerals and the aqueous phase, (2) CO2 solubility dependence on pressure, temperature and salinity of the system, and (3) redox processes that could be important in deep subsurface environments. The geochemical evolution under CO2 injection conditions was evaluated. In addition, changes in porosity were monitored during the simulations. Results indicate that CO2 sequestration by matrix minerals varies considerably with rock type. Under favorable conditions the amount of CO2 that may be sequestered by precipitation of secondary carbonates is comparable with and can be larger than the effect of CO2 dissolution in pore waters. The precipitation of ankerite and siderite is sensitive to the rate of reduction of Fe(III) mineral precursors such as goethite or glauconite. The accumulation of carbonates in the rock matrix leads to a considerable decrease in porosity. This in turn adversely affects permeability and fluid flow in the aquifer. The numerical experiments described here provide useful insight into sequestration mechanisms, and their controlling geochemical conditions and parameters.  相似文献   

3.
归纳了新疆塔什库尔干谷地地热地质条件,分析了区内地质构造、地温分布、地热流体化学及同位素特征,研究了地热形成机理,计算了曲曼地热田的地热资源量和可开采量。结果表明: 研究区地热资源受断裂构造控制; 地温变化与盖层、完整基岩、断裂带(热储)表现出明显的一致性,目前实测最高热储温度为161 ℃,深部热储计算温度可达222~268 ℃,地温梯度最高为149.20 ℃/100 m; 地热流体具有深循环特征,与浅表冷水的水化学和同位素特征具有明显的差异; 地热流体来源于大气降水,在断裂及裂隙内储存、运移、富集,在侵入岩体放射性生热和结晶余热的热量供应下,地下流体不断与围岩进行热量及物质交换,在热储围岩和盖层中,热量以传导方式为主,在热储内,热量以对流方式为主; 曲曼地热田储存的热量为55.919×1011 MJ,地热流体可开采量约为12 593 m3/d,产能(热能)约为77.9 MW。因此认为,塔什库尔干谷地热储埋藏深度浅,易开采,具有可观的直接和间接经济价值。  相似文献   

4.
This study focused on typical injection layers of deep saline aquifers in the Shiqianfeng Formation used in the Carbon Capture and Sequestration Demonstration Projects in the Ordos Basin, Northwest China. The study employed experiments and numerical simulations to investigate the mechanism of CO2 mineral sequestration in these deep saline aquifers. The experimental results showed that the dissolved minerals are plagioclase, hematite, illite–smectite mixed layer clay and illite, whereas the precipitated minerals are quartz (at 55, and 70 °C) and kaolinite (at 70 °C). There are rare carbonate mineral precipitations at the experimental time scale, while the precipitation of quartz as a product of the dissolution of silicate minerals and some intermediate minerals rich in K and Mg that transform to clay minerals, reveals the possibility of carbonate precipitation at the longer time scale. These results are consistent with some results previously reported in the literature. We calibrated the kinetic parameters of mineral dissolution and precipitation by these experimental results and then simulated the CO2 mineral sequestration under deep saline aquifer conditions. The simulation results showed that the dissolved minerals are albite, anorthite and minor hematite, whereas the precipitated minerals are calcite, kaolinite and smectite at 55 and 70 °C. The geochemical reaction of illite is more complex. At 55 °C, illite is dissolved at the relatively lag time and transformed to dawsonite; at 70 °C, illite is precipitated in the early reaction period and then transformed to kaolinite. Based on this research, sequestrated CO2 minerals, which are mainly related to the temperature of deep saline aquifers in Shiqianfeng Fm., are calcite and dawsonite at lower temperature, and calcite at higher temperature. The simulation results also establish that calcite could precipitate over a time scale of thousands of years, and the higher the temperature the sooner such a process would occur due to increased reaction rates. These characteristics are conducive, not only to the earlier occurrence of mineral sequestration, but also increase the sequestration capacity of the same mineral components. For a sequestration period of 10,000 years, we determined that the mineral sequestration capacity is 0.786 kg/m3 at 55 °C, and 2.180 kg/m3 at 70 °C. Furthermore, the occurrence of mineral sequestration indirectly increases the solubility of CO2 in the early reaction period, but this decreases with the increase in temperature.  相似文献   

5.
Geothermal water is plentiful in Changbai Mountain region, northeastern China, due to the volcanic activities and widespread faults. For the exploration of geothermal resources, this study uses quartz and cation geothermometer to estimate the temperatures of the geothermal reservoir and uses the tubular models to evaluate the thermal gradient. The hydrogeochemical characteristics of the geothermal resources were also evaluated by hydrogeochemical analysis. The results showed that the geothermal reservoir temperatures of the four major thermal springs in Changbai Mountain region range from 72 to 169 °C. The average geothermal reservoir temperatures of Jinjiang hot springs, Changbai hot springs I, Xianrenqiao hot springs, and Changbai hot springs II are 129.25, 169, 89, and 73.67 °C, respectively. The geothermal gradient values of the four major thermal springs have different characteristics. The geothermal gradient values of Jinjiang hot springs and Changbai hot springs I are 4.6 and 3.1 °C/100 m, respectively. The geothermal gradient values of Xianrenqiao thermal springs and Changbai thermal springs II are both lower than 1.5 °C/100 m, with the values of 1.1 and 1.4 °C/100 m. And the geothermal gradients are influenced by Changbai Mountain Tianchi volcano. In addition, the water chemical analyses showed that the geothermal water types are HCO3-Na with higher concentrations of Na+, Cl?, SO4 2?, TDS, and HCO3 ? than the non-thermal waters, which suggested a deep and long water cycle of the thermal water, and therefore a sufficient water-rock interaction.  相似文献   

6.
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.  相似文献   

7.
The potential for metal release associated with CO2 leakage from underground storage formations into shallow aquifers is an important consideration in assessment of risk associated with CO2 sequestration. Metal release can be driven by acidification of groundwaters caused by dissolution of CO2 and subsequent dissociation of carbonic acid. Thus, acidity is considered one of the main drivers for water quality degradation when evaluating potential impacts of CO2 leakage. Dissolution of carbonate minerals buffers the increased acidity. Thus, it is generally thought that carbonate aquifers will be less impacted by CO2 leakage than non-carbonate aquifers due to their high buffering potential. However, dissolution of carbonate minerals can also release trace metals, often present as impurities in the carbonate crystal structure, into solution. The impact of the release of trace metals through this mechanism on water quality remains relatively unknown. In a previous study we demonstrated that calcite dissolution contributed more metal release into solution than sulfide dissolution or desorption when limestone samples were dissolved in elevated CO2 conditions. The study presented in this paper expanded our work to dolomite formations and details a thorough investigation on the role of mineral composition and mechanisms on trace element release in the presence of CO2. Detailed characterization of samples from dolomite formations demonstrated stronger associations of metal releases with dissolution of carbonate mineral phases relative to sulfide minerals or surface sorption sites. Aqueous concentrations of Sr2+, CO2+, Mn2+, Ni2+, Tl+, and Zn2+ increased when these dolomite rocks were exposed to elevated concentrations of CO2. The aqueous concentrations of these metals correlate to aqueous concentrations of Ca2+ throughout the experiments. All of the experimental evidence points to carbonate minerals as the dominant source of metals from these dolomite rocks to solution under experimental CO2 leakage conditions. Aqueous concentrations of Ca2+ and Mg2+ predicted from numerical simulation of kinetic dolomite dissolution match those observed in the experiments when the surface area is three to five orders of magnitude lower than the surface area of the samples measured by gas adsorption.  相似文献   

8.
Shallow geothermal prospecting ( < 700 m) has been performed in four zones in Morocco for which few deep data are available: northwestern basin, northeastern basin, Tadla Basin and Agadir Basin. These areas are different geologically and hydrogeologically. The temperature data from 250 wells at depths between 15 and 500 m have been analysed in order to estimate the natural geothermal gradient in these areas, to determine the principal thermal anomalies, to identify the main thermal indices and to characterise the recharge, discharge and potential mixing limits of the aquifers.The hydrostratigraphical study of each basin revealed several potential reservoir layers in which the Turonian carbonate aquifer (Tadal and Agadir Basins) and Liassic acquifer (Moroccan northwestern and northeastern basins) are the most important hot water reservoirs in Morocco. The recharge zones of each aquifer are characterised by high topography, high water potential, shallow cold water, low geothermal gradient and negative anomalies. The discharge zones are characterized by low topography, low piezometric level, high geothermal gradient, high temperature with hot springs and positive anomalies. The main thermal indices and the principal thermal anomalies that coincide with the artesian zones of the Turonian and Liassic aquifers have been identified.  相似文献   

9.
Carbon dioxide enhanced oil recovery (CO2-EOR) has been widely applied to the process of carbon capture, utilization, and storage (CCUS). Here, we investigate CO2–oil–water–rock interactions under reservoir conditions (100 °C and 24 MPa) in order to understand the fluid–rock interactions following termination of a CO2-EOR project. Our experimental results show that CO2-rich fluid remained the active fluid controlling the dissolution–precipitation processes in an oil-undersaturated sandstone reservoir; e.g., the dissolution of feldspar and calcite, and the precipitation of kaolinite as well as solid phases comprising O, Si, Al, Na, C, and Ti. Mineral dissolution rates were reduced in the case that mineral surfaces were coated by oil. Mineral wettability and composition, and oil saturation were the main controls on the exposed surface area of grains, and mineral wettability in particular led to selective dissolution. In addition, the permeability of the reservoir decreased substantially due to the precipitation of kaolinite and solid-phase particles, and due to the clogging of less soluble mineral particles released by the dissolution of K-feldspar and carbonate cement, whereas porosity increased. The results provide insight into potential formation damage resulting from CO2-EOR projects.  相似文献   

10.
Deep saline aquifers are considered as the most promising option for geologic disposal of CO2. One of the main concerns, however, is the integrity of the caprocks between and above the storage formations. Here, a hydrogeochemical and isotopic investigation is presented, using ionic chemistry, stable isotopes (δ18O, δ2H and 87Sr/86Sr) and radiocarbon dating, on five saline aquifers on a regional scale, namely: Neogene Minghuazhen, Guantao, Ordivician, Cambrian and Precambrian, all found in the Bohai Bay Basin (BBB) in North China. Groundwater recharge, flow pattern, age and mixing processes in the saline aquifers show that the Neogene Guantao Formation (Ng) in the Jizhong and Huanghua Depressions on both of the west and east sides of the Cangxian Uplift is a prospective reservoir for CO2 sequestration, with a well confined regional seal above, which is the clayey layers in the Neogene Minghuazhen Formation (Nm). However, this is not the case in the Cangxian Uplift, where the Ng is missing where structural high and fault zones are developed, creating strong hydraulic connections and trans-formational flow to the Nm aquifer. Comparing storage capacity and long-term security between the various hydrogeologic units, the depressions are better candidate sites for CO2 sequestration in the BBB.  相似文献   

11.
To assess CO2 underground sequestration from a geochemical viewpoint, the anorthite dissolution rate, which is an important parameter of risk analysis, was measured in a CO2–water system. The authors sought to obtain precise dissolution rate data in a short time observing a crystal surface on a nanoscale. For this purpose, phase-shift interferometry was applied. Using this method, uncertainty of the reactive surface area that is imparted on calculation of the dissolution rate constant can also be avoided. The time-course profile of vertical retreat of the surface revealed that the anorthite dissolution process changes from the initial transient state to a later steady state, which is consistent with results of numerous precedent studies. The transient dissolution rate depends strongly on local features (e.g., density of defects, variation of chemical compositions) of the crystal surface, rather than on temperature. Therefore, it is very important to determine the original properties of the anorthite surface for the examination of subsequent dissolution process. Contrary to general expectations, the anorthite dissolution can alter the physical properties of reservoir rock immediately after CO2 injection. The simple estimation using the anorthite dissolution rate obtained in this study, which was done as a test case for the CO2 underground sequestration project conducted by RITE, revealed that porosity of reservoir rock increased about 2% (23–23.4%) of initial values during 60 a. That change in physical property in such a short time might enhance the diffusion of injected CO2 and formation water, and therefore accelerate further geochemical reactions. Results of this study demonstrate that the geochemical water–rock interaction, which is generally regarded as a longer-term phenomenon than various physical processes, can also affect the reservoir system from the initial stage.  相似文献   

12.
Reservoir and cap-rock core samples with variable lithology's representative of siliciclastic reservoirs used for CO2 storage have been characterized and reacted at reservoir conditions with an impure CO2 stream and low salinity brine. Cores from a target CO2 storage site in Queensland, Australia were tested. Mineralogical controls on the resulting changes to porosity and water chemistry have been identified. The tested siliciclastic reservoir core samples can be grouped generally into three responses to impure CO2-brine reaction, dependent on mineralogy. The mineralogically clean quartzose reservoir cores had high porosities, with negligible change after reaction, in resolvable porosity or mineralogy, calculated using X-ray micro computed tomography and QEMSCAN. However, strong brine acidification and a high concentration of dissolved sulphate were generated in experiments owing to minimal mineral buffering. Also, the movement of kaolin has the potential to block pore throats and reduce permeability. The reaction of the impure CO2-brine with calcite-cemented cap-rock core samples caused the largest porosity changes after reaction through calcite dissolution; to the extent that one sample developed a connection of open pores that extended into the core sub-plug. This has the potential to both favor injectivity but also affect CO2 migration. The dissolution of calcite caused the buffering of acidity resulting in no significant observable silicate dissolution. Clay-rich cap-rock core samples with minor amounts of carbonate minerals had only small changes after reaction. Created porosity appeared mainly disconnected. Changes were instead associated with decreases in density from Fe-leaching of chlorite or dissolution of minor amounts of carbonates and plagioclase. The interbedded sandstone and shale core also developed increased porosity parallel to bedding through dissolution of carbonates and reactive silicates in the sandy layers. Tight interbedded cap-rocks could be expected to act as baffles to fluids preventing vertical fluid migration. Concentrations of dissolved elements including Ca, Fe, Mn, and Ni increased during reactions of several core samples, with Mn, Mg, Co, and Zn correlated with Ca from cap-rock cores. Precipitation of gypsum, Fe-oxides and clays on seal core samples sequestered dissolved elements including Fe through co-precipitation or adsorption. A conceptual model of impure CO2-water-rock interactions for a siliciclastic reservoir is discussed.  相似文献   

13.
兀少波  邵睿涛 《地下水》2020,(1):112-115,282
扶风县城位于渭河盆地咸礼凸起西部,地热资源包括新生界碎屑岩类孔隙型地热资源和下古生界碳酸盐岩类岩溶型地热资源,地热资源条件较好。以扶风佛文化休闲产业园R2地热井为研究对象,采用钢齿牙轮钻头、PDC钻头和镶齿牙轮钻头分别对新生界松散地层和下古生界碳酸盐岩地层进行钻进,建立成井深度为1 900m的二级成井结构,对区域地热资源条件与成井工艺进行研究,结果可知:该地热井取用的新近系上新统蓝田-灞河组热储层、中新统高陵群热储层和下古生界奥陶系热储层为目的层,取水段为923. 3~1 874. 2 m,经产能测试,该井抽水降深40. 8 m时,出水量64. 11 m^3/h,井口水温66℃。按GB/T11615-2010《地热资源地质勘查规范》,扶风县城地热资源属于较适宜开采区;地热资源温度分级属于热水,可用于采暖、理疗、洗浴、温室等;地热水中氟、偏硼酸、偏硅酸、氡等矿物含量具有医疗价值,其中氟含量达到命名矿水浓度,可命名为氟水,具有较高的理疗价值。  相似文献   

14.
Thermal water of Thermopylae and from other geothermal fields located in the southern part of the Sperchios basin (central Greece) are characterized by high salinity (total dissolved salts, or TDS, range from 1.2 to 30.3 g L−1) associated with a degassing of CO2. To determine the mineralization processes, geochemical and isotopic investigations (major elements, 18O, 2H and 13C) have been carried out upon 17 thermal waters from springs and boreholes. This study emphasizes that all the thermal waters result from the mixing of a seawater end-member, several fresh water components depending on the field location, and a mantle-derived CO2 rising upward through an E–W fault system. The seawater identified in the thermal mixture is likely to be evolved Aegean seawater (ASW). Once intruded into the basin sediments, the trapped seawater has its chemical content modified by both water–rock interactions and massive dissolution of the deep CO2 (pCO2 of 100.5 atm). The modelling performed with PHREEQC indicates that the anomalous major ion ratios measured in the so-called evolved ASW are explained by the dissolution of calcite and dolomitization process associated to precipitation of gypsum within the thermal aquifer.  相似文献   

15.
朱喜  王贵玲  马峰  张薇  张庆莲  张汉雄 《地球科学》2021,46(7):2594-2608
雄安新区蓟县系雾迷山组热储层中具有丰富的中低温地热资源,研究其地热流体水文地球化学特征可分析地热资源的形成机制,对推动雄安新区深部地热资源有效开发利用具有重要意义.太行山区雾迷山组为基岩裸露区,雄安新区雾迷山组基底埋藏较深,两个系统的地热流体经历不同的水岩相互作用,导致水化学特征有一定差异.通过对保定以西太行山区-雄安新区共26组蓟县系雾迷山组地热流体样品的水化学及同位素数据进行分析,研究地热流体的补给来源及经历的深部地热循环过程.太行山区雾迷山组流体水化学类型以HCO3-Ca·Mg型为主,雄安新区以Cl·HCO3-Na型为主.地热流体均来源于大气降水,通过断裂、裂隙等通道入渗,在长距离运移过程中伴随有矿物的沉淀和溶解现象,水岩相互作用逐渐增强.深部热循环深度为2 880.26~4 143.42 m,均值为3 700 m,深部热储温度为160℃左右;地热流体在深部通过断裂上升过程中,由于传导冷却、冷水混入及深部热源通过结晶基底的热传导作用,在750~2 100 m的凸起处雾迷山组碳酸盐岩地层中封闭聚集形成热储层,热储平均温度为70℃左右,属于对流-传导型地热系统.   相似文献   

16.
辽宁丹东地区地热资源丰富,阐明其地热田的成因模式对于区域热水资源的可持续开发利用具有重要意义。以区内北汤、东汤、五龙背地热田为研究对象,进行水化学和同位素分析。结果表明,北汤、东汤、五龙背地热水的水化学类型分别为SO4·Cl-Na·Ca型、HCO3·SO4-Na型、 HCO3-Na·Ca、HCO3·SO4-Na和HCO3·Cl-Na型。研究区的热水来源为大气降水,北汤、东汤地热田的补给高程分别为678 m和376 m。根据14C测年方法,得出北汤、东汤和五龙背地热田地热水年龄分别为2 000~3 300 a B.P.、2 200~7 200 a B.P.和700~2 900 a B.P.。根据二氧化硅地温计和lg(Q/K)方法,北汤、东汤和五龙背地热田的热储温度分别为92 ℃、120 ℃和100~101 ℃,相应的地热水循环深度分别为1 900 m、3 000 m和800~1 800 m。地热水接收大气降水入渗补给,经断裂带深循环加热,于NNE和NW向两组断裂交汇处上涌进入浅部含水层或出露地表成泉,属中低温对流型地热系统。  相似文献   

17.
The injection of CO2 into deep saline aquifers is being considered as an option for greenhouse gas mitigation. However, the response of an aquifer to the injected CO2 is largely unknown. Experiments involving the reaction of Navajo Sandstone with acidic brine were conducted at 200°C and 25 or 30 MPa to evaluate the extent of fluid–rock interactions. The first experiment examined sandstone interaction with CO2-impregnated brine; the second experiment examined sandstone dissolution in CO2-free acidic brine; the third one is carried out in a mixed-flow reactor and designed to measure sandstone dissolution rates based on time-series Si concentrations. The solution chemistry data indicate that the SiO2(aq) increases gradually and pH increases slowly with reaction progress. Silicate minerals in the sandstone display textures (dissolution features, secondary mineralization), indicating that these phases are reacting strongly with the fluid. Dissolution of feldspars and conversion of smectite to illite are likely to be the two reactions that contribute to the release of SiO2(aq). The product minerals present at the end of the experiments are illite, illite/smectite, allophane, and carbonate minerals (for the CO2-charged system). Dissolved CO2 is likely to acidify the brine and to provide a source of carbon for the precipitation of carbonate minerals. Mineral trapping through the precipitation of carbonate minerals is favored thermodynamically and was observed in the experiments. The chemical reactions likely increase the bulk porosity of the sandstone due to dissolution of silicate minerals. However, allophane and illite/smectite fill voids in sandstone grains. There is no evidence for the removal of clay coatings due to chemical reactions. It is uncertain whether the mechanical forces near an injection well would mobilize the smectite and allophane and clog pore throats. Trace amounts of metals, including Cu, Zn, and Ba, were mobilized.  相似文献   

18.
Sequestration of CO2 into a deep geological reservoir causes a complex interaction of different processes such as multiphase flow, phase transition, multicomponent transport, and geochemical reactions between dissolved CO2 and the mineral matrix of the porous medium. A prognosis of the reservoir behaviour and the feedback from large-scale geochemical alterations require efficient process-based numerical models. For this purpose, the multiphase flow and multicomponent transport code OpenGeoSys-Eclipse have been coupled to the geochemical model ChemApp. The newly developed coupled simulator was successfully verified for correctness and accuracy of the implemented reaction module by benchmarking tests. The code was then applied to assess the impact of geochemical reactions during CO2 sequestration at a hypothetical but typical Bunter sandstone formation in the Northern German Basin. Injection and spreading of 1.48 × 107 t of CO2 in an anticline structure of the reservoir were simulated over a period of 20 years of injection plus 80 years of post-injection time. Equilibrium geochemical calculations performed by ChemApp show only a low reactivity to the geochemical system. The increased acidity of the aqueous solution results in dissolution of small amounts of calcite, anhydrite, and quartz. Geochemical alterations of the mineral phase composition result in slight increases in porosity and permeability, which locally may reach up to +0.02 and 0.1 %, respectively.  相似文献   

19.
《Applied Geochemistry》2000,15(8):1085-1095
The pore space of deep saline aquifers in the Alberta (sedimentary) Basin offers a significant volume for waste storage by “hydrodynamic trapping”. Furthermore, given the slow regional fluid flow in these deep saline aquifers, ample time exists for waste-water/rock chemical reactions to take place. A geochemical computer model (PATHARC) was used to compute the interaction of industrial waste streams comprising CO2, H2SO4 and H2S with the minerals in typical carbonate and sandstone aquifers from the Alberta Basin. The results support the idea that these acids can be neutralized by such reactions and that new mineral products are formed, such as calcite, siderite, anhydrite/gypsum and pyrrhotite, thereby trapping the CO3, SO4 and S ions that are formed when the acid gases dissolve in the formation water. Siliciclastic aquifers appear to be a better host for “mineral trapping” than carbonate aquifers, especially with regard to CO2. Carbonate aquifers may be more prone to leakage due to high CO2 pressures generated by reaction with H2SO4 and H2S. Even though permeability decreases are expected due to this “mineral trapping”, they can be partially controlled so that plugging of the aquifer does not occur.  相似文献   

20.
富CO_2流体-砂岩相互作用是砂岩储层次生孔隙的重要形成机制。苏北黄桥地区作为中国重要的CO_2气产区,富CO_2流体对上二叠统龙潭组砂岩储层的改造问题备受关注。为揭示富CO_2流体的作用特征及其对储层的影响,对黄桥地区典型钻井开展了系统的岩心描述和岩矿鉴定,并进行了微区原位观测和相关地球化学分析。结果表明,在靠近CO_2流体活动强烈的断裂带部位(特别是断层上盘),砂岩中碳酸盐胶结物基本溶蚀殆尽,仅存少量交代成因菱铁矿,同时钾长石类碎屑溶蚀非常强烈,并伴随高岭石等矿物沉淀,以及石英次生加大,还发育片钠铝石等指示高浓度CO_2作用的特征矿物,形成与CO_2流体作用相关的特征矿物组合(片钠铝石+高岭石+次生石英+菱铁矿);而在远离断裂的部位,受CO_2流体影响较弱,溶蚀作用也较弱,有较多的次生方解石沉淀,形成了以方解石+菱铁矿为主的自生矿物组合。前者次生孔隙发育,后者则更加致密。据此提出了深源断裂主控下与富CO_2流体作用相关的储层发育模式,为油气勘探和开发提供了新的思路。  相似文献   

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