scholarly journals Red-bed bleaching in a CO2 storage analogue: Insights from Entrada Sandstone fracture-hosted mineralization

2020 ◽  
Vol 90 (1) ◽  
pp. 48-66
Author(s):  
Jeremy C. Rushton ◽  
Doris Wagner ◽  
Jonathan M. Pearce ◽  
Christopher A. Rochelle ◽  
Gemma Purser
Keyword(s):  
Time Scales ◽  
Co2 Storage ◽  
Pyrite Oxidation ◽  
Carbon Capture And Storage ◽  
Spatial Relationship ◽  
Oxidation Reactions ◽  
Geological Time ◽  
Genetic Link ◽  
Geological Processes ◽  
Red Bed

ABSTRACT Improving our ability to predict the interactions between CO2 and reservoir rocks at geological time scales is of key importance if carbon capture and storage (CCS) is to have a role in climate-change mitigation, particularly in the light of likely regulatory requirements. Understanding and identifying the relevant geological processes over long time scales can be obtained only at natural-analogue sites. At one such site, in the Salt Wash Graben area of Utah, USA, widespread bleaching affects the Middle Jurassic red-bed “wet dune” Entrada Sandstone. Previous work has proposed a genetic link between the bleaching and spatially concomitant recent and modern CO2-rich fluids. The results presented here challenge some of the previous models and come from a detailed petrographic examination of mineralized fractures in the Entrada Sandstone that are centered in vertical extensions to the bleaching. These fractures typically contain complex mineralization assemblages. Pyrite was a paragenetically early phase, identifiable from common pseudomorphs of mixed iron oxides and oxyhydroxides that rarely contain relict pyrite. The pyrite contains up to 3 wt% arsenic. The volume of fracture-adjacent bleached sandstone is sufficient to have been the source of iron for the pyrite originally present in the fracture. The pyrite pseudomorphs occur at the center of fracture- and pore-filling cements that comprise intergrowths of hematite–goethite–jarosite–gypsum, an assemblage that suggests that their formation resulted from the oxidative alteration of pyrite, a genetic link supported by the arsenic present in the iron-bearing minerals. The presence of jarosite and proximal removal of earlier, sandstone-hosted carbonates are consistent with, and indicative of, the low-pH conditions associated with pyrite oxidation reactions. Calcite- and gypsum-cemented fractures crosscut, and contain fragments of, the pyrite-pseudomorphic and -oxidation assemblages, proving that they postdate pyrite formation and its subsequent oxidation, and that pyrite oxidation was not a result of modern weathering reactions. In outcrop, some calcite- and gypsum-cemented fractures link with travertine deposits associated with the modern and recent CO2-rich fluids. The mineral assemblages observed here, and the paragenetic sequence that we have inferred, suggest that the fracture-associated bleaching patterns result from the fracture-fed movement of sulfur-bearing reducing fluids, with hydrogen sulfide the most likely bleaching agent. We conclude that bleaching adjacent to fractures is not genetically related to modern CO2-bearing fluids despite the spatial relationship. The bleaching was already present when the modern fluids utilized the same fracture-based fluid pathways. We suggest that the more widespread regional bleaching formed contemporaneously with the fracture bleaching and followed similar mechanisms. This study highlights the complexity of interpreting analogue sites and the importance of using field and petrographic observations to unravel textures and events that are juxtaposed spatially but not temporally.

Carbonation possibilities of Steel slags -- a review

2021 ◽  
Author(s):  
Raghavendra Ragipani ◽  
Sankar Bhattacharya ◽  
Akkihebbal K. Suresh
Keyword(s):  
Carbon Dioxide ◽  
Time Scales ◽  
Carbon Dioxide Sequestration ◽  
Mineral Carbonation ◽  
Geological Time ◽  
The Stability ◽  
Significant Attention

Research pertaining to carbon dioxide sequestration via mineral carbonation has gained significant attention, primarily due to the stability of sequestered \ce{CO2} over geological time scales. Use of industry-derived alkaline wastes...

Experimental and Modeling Study of Salt Precipitation During Injection of CO2 Contaminated With H2S Into Depleted Gas Fields in the Northeast of the Netherlands

SPE Journal ◽  
2014 ◽  
Vol 19 (06) ◽  
pp. 1058-1068 ◽  
Author(s):  
P.. Bolourinejad ◽  
R.. Herber
Keyword(s):  
The Netherlands ◽  
Carbonic Acid ◽  
Co2 Storage ◽  
Mineral Dissolution ◽  
Co2 Injection ◽  
Salt Precipitation ◽  
Geological Time ◽  
Core Samples ◽  
Carbon Dioxide Co2 ◽  
Gas Fields

Summary Depleted gas fields are among the most probable candidates for subsurface storage of carbon dioxide (CO2). With proven reservoir and qualified seal, these fields have retained gas over geological time scales. However, unlike methane, injection of CO2 changes the pH of the brine because of the formation of carbonic acid. Subsequent dissolution/precipitation of minerals changes the porosity/permeability of reservoir and caprock. Thus, for adequate, safe, and effective CO2 storage, the subsurface system needs to be fully understood. An important aspect for subsurface storage of CO2 is purity of this gas, which influences risk and cost of the process. To investigate the effects of CO2 plus impurities in a real case example, we have carried out medium-term (30-day) laboratory experiments (300 bar, 100°C) on reservoir and caprock core samples from gas fields in the northeast of the Netherlands. In addition, we attempted to determine the maximum allowable concentration of one of the possible impurities in the CO2 stream [hydrogen sulfide (H2S)] in these fields. The injected gases—CO2, CO2+100 ppm H2S, and CO2+5,000 ppm H2S—were reacting with core samples and brine (81 g/L Na+, 173 g/L Cl−, 22 g/L Ca2+, 23 g/L Mg2+, 1.5 g/L K+, and 0.2 g/L SO42−). Before and after the experiments, the core samples were analyzed by scanning electron microscope (SEM) and X-ray diffraction (XRD) for mineralogical variations. The permeability of the samples was also measured. After the experiments, dissolution of feldspars, carbonates, and kaolinite was observed as expected. In addition, we observed fresh precipitation of kaolinite. However, two significant results were obtained when adding H2S to the CO2 stream. First, we observed precipitation of sulfate minerals (anhydrite and pyrite). This differs from results after pure CO2 injection, where dissolution of anhydrite was dominant in the samples. Second, severe salt precipitation took place in the presence of H2S. This is mainly caused by the nucleation of anhydrite and pyrite, which enabled halite precipitation, and to a lesser degree by the higher solubility of H2S in water and higher water content of the gas phase in the presence of H2S. This was confirmed by the use of CMG-GEM (CMG 2011) modeling software. The precipitation of halite, anhydrite, and pyrite affects the permeability of the samples in different ways. After pure CO2 and CO2+100 ppm H2S injection, permeability of the reservoir samples increased by 10–30% and ≤3%, respectively. In caprock samples, permeability increased by a factor of 3–10 and 1.3, respectively. However, after addition of 5,000 ppm H2S, the permeability of all samples decreased significantly. In the case of CO2+100 ppm H2S, halite, anhydrite, and pyrite precipitation did balance mineral dissolution, causing minimal variation in the permeability of samples.

scholarly journals Managing Uncertainty in Geological CO2 Storage Using Bayesian Evidential Learning

Energies ◽  
2021 ◽  
Vol 14 (6) ◽  
pp. 1557
Author(s):  
Amine Tadjer ◽  
Reidar B. Bratvold
Keyword(s):  
Uncertainty Quantification ◽  
History Matching ◽  
Co2 Storage ◽  
Carbon Capture And Storage ◽  
Monitoring Program ◽  
Co2 Injection ◽  
Drinking Water Contamination ◽  
Model Inversion ◽  
Geological Co2 Storage ◽  
And Storage

Carbon capture and storage (CCS) has been increasingly looking like a promising strategy to reduce CO2 emissions and meet the Paris agreement’s climate target. To ensure that CCS is safe and successful, an efficient monitoring program that will prevent storage reservoir leakage and drinking water contamination in groundwater aquifers must be implemented. However, geologic CO2 sequestration (GCS) sites are not completely certain about the geological properties, which makes it difficult to predict the behavior of the injected gases, CO2 brine leakage rates through wellbores, and CO2 plume migration. Significant effort is required to observe how CO2 behaves in reservoirs. A key question is: Will the CO2 injection and storage behave as expected, and can we anticipate leakages? History matching of reservoir models can mitigate uncertainty towards a predictive strategy. It could prove challenging to develop a set of history matching models that preserve geological realism. A new Bayesian evidential learning (BEL) protocol for uncertainty quantification was released through literature, as an alternative to the model-space inversion in the history-matching approach. Consequently, an ensemble of previous geological models was developed using a prior distribution’s Monte Carlo simulation, followed by direct forecasting (DF) for joint uncertainty quantification. The goal of this work is to use prior models to identify a statistical relationship between data prediction, ensemble models, and data variables, without any explicit model inversion. The paper also introduces a new DF implementation using an ensemble smoother and shows that the new implementation can make the computation more robust than the standard method. The Utsira saline aquifer west of Norway is used to exemplify BEL’s ability to predict the CO2 mass and leakages and improve decision support regarding CO2 storage projects.

Milankovitch cycles and their effects on species in ecological and evolutionary time

Paleobiology ◽  
1990 ◽  
Vol 16 (1) ◽  
pp. 11-21 ◽  
Author(s):  
K. D. Bennett
Keyword(s):  
Time Scales ◽  
Climatic Changes ◽  
Milankovitch Cycles ◽  
Mass Extinctions ◽  
Geological Time ◽  
Evolutionary Time ◽  
Abiotic Environment ◽  
Earth History ◽  
Microevolutionary Change ◽  
Second Tier

The Quaternary ice ages were paced by astronomical cycles with periodicities of 20–100 k.y. (Milankovitch cycles). These cycles have been present throughout earth history. The Quaternary fossil record, marine and terrestrial, near to and remote from centers of glaciation, shows that communities of plants and animals are temporary, lasting only a few thousand years at the most. Response of populations to the climatic changes of Quaternary Milankovitch cycles can be taken as typical of the way populations have behaved throughout earth history. Milankovitch cycles thus force an instability of climate and other aspects of the biotic and abiotic environment on time scales much less than typical species durations (1–30 m.y.). Any microevolutionary change that accumulates on a time scale of thousands of years is likely to be lost as communities are reorganized following climatic changes. A four-tier hierarchy of time scales for evolutionary processes can be constructed as follows: ecological time (thousands of years), Milankovitch cycles (20–100 k.y.), geological time (millions of years), mass extinctions (approximately 26 m.y.). “Ecological time” and “geological time” are defined temporally as the intervals between events of the second and fourth tiers, respectively. Gould's (1985) “paradox of the first tier” can be resolved, at least in part, through the undoing of Darwinian natural selection at the first tier by Milankovitch cycles at the second tier.

scholarly journals The potential for large-scale, subsurface geological CO2 storage in Denmark

1969 ◽  
Vol 17 ◽  
pp. 13-16 ◽  
Author(s):  
Peter Frykman ◽  
Lars Henrik Nielsen ◽  
Thomas Vangkilde-Pedersen
Keyword(s):  
Carbon Capture ◽  
Large Scale ◽  
Best Practice ◽  
Co2 Storage ◽  
Carbon Capture And Storage ◽  
The European Union ◽  
Geological Storage ◽  
Geological Co2 Storage ◽  
Research Programmes ◽  
Capture Techniques

Carbon capture and storage (CCS) is increasingly considered to be a tool that can significantly reduce the emission of CO2. It is viewed as a technology that can contribute to a substantial, global reduction of emitted CO2 within the timeframe that seems available for mitigating the effects of present and continued emission. In order to develop the CCS method the European Union (EU) has supported research programmes for more than a decade, which focus on capture techniques, transport and geological storage. The results of the numerous research projects on geological storage are summarised in a comprehensive best practice manual outlining guidelines for storage in saline aquifers (Chadwick et al. 2008). A detailed directive for geological storage is under implementation (European Commission 2009), and the EU has furthermore established a programme for supporting the development of more than ten large-scale demonstration plants throughout Europe. Geological investigations show that suitable storage sites are present in most European countries. In Denmark initial investigations conducted by the Geological Survey of Denmark and Greenland and private companies indicate that there is significant storage potential at several locations in the subsurface.

scholarly journals Valorization of OFMSW Digestate-Derived Syngas toward Methanol, Hydrogen, or Electricity: Process Simulation and Carbon Footprint Calculation

Processes ◽  
2020 ◽  
Vol 8 (5) ◽  
pp. 526 ◽  
Author(s):  
Aristide Giuliano ◽  
Enrico Catizzone ◽  
Cesare Freda ◽  
Giacinto Cornacchia
Keyword(s):  
Hydrogen Production ◽  
Process Simulation ◽  
Carbon Capture ◽  
Combustion Engine ◽  
Co2 Storage ◽  
Carbon Capture And Storage ◽  
Simulation Software ◽  
Added Value ◽  
Electricity Production ◽  
Methanol Production

This paper explores a possible waste-based economy transition strategy. Digestate from the organic fraction of municipal solid waste (OFMSW) is considered, as well as a low-added value product to be properly valorized. In this regard, air gasification may be used to produce syngas. In this work, the production of methanol, hydrogen, or electricity from digestate-derived syngas was assessed by ChemCAD process simulation software. The process scheme of methanol production comprises the following parts: water gas shift (WGS) with carbon capture and storage units (CCS), methanol synthesis, and methanol purification. In the case of hydrogen production, after WGS-CCS, hydrogen was purified from residual nitrogen by pressure swing absorption (PSA). Finally, for electricity production, the digestate-derived syngas was used as fuel in an internal combustion engine. The main objective of this work is to compare the proposed scenarios in terms of CO2 emission intensity and the effect of CO2 storage. In particular, CCS units were used for methanol or hydrogen production with the aim of obtaining high equilibrium yield toward these products. On the basis of 100 kt/year of digestate, results show that the global CO2 savings were 80, 71, and 69 ktCO2eq/year for electricity, methanol, and hydrogen production, respectively. If carbon storage was considered, savings of about 105 and 99 ktCO2eq/year were achieved with methanol and hydrogen production, respectively. The proposed scenarios may provide an attractive option for transitioning into methanol or hydrogen economy of the future.

Experimental fluid-mediated alteration of zircon under lower greenschist facies conditions

2020 ◽  
Vol 58 (2) ◽  
pp. 247-265
Author(s):  
Colter J. Kelly ◽  
Daniel E. Harlov ◽  
David A. Schneider ◽  
Simon E. Jackson ◽  
Renelle Dubosq
Keyword(s):  
Ion Exchange ◽  
Inductively Coupled Plasma ◽  
Earth Science ◽  
Science Research ◽  
Aqueous Fluid ◽  
Mapping Technique ◽  
Geological Time ◽  
Geological Time Scale ◽  
Chemically Modified ◽  
Geological Processes

ABSTRACT The use of zircon in the dating of geological processes and tectonic events has become a standard approach in many aspects of Earth science research. As a result, understanding how zircon interacts with aqueous fluids during metasomatism has become increasingly important. The alteration of natural zircon is driven primarily by coupled dissolution–reprecipitation or by ion-exchange with an aqueous fluid. In this study, whole and intact, euhedral light-brown zircon crystals (100–250 μm in length; 2 mg) from the Oligocene Fish Canyon Tuff (FCT) were experimentally reacted with an alkali-bearing reactive fluid and a REE + P source (0.5 mg CePO4 or 0.5 mg YPO4). Experiments were conducted in sealed Au metal capsules at 350 °C and 100 MPa for 182 days. During the experiment, the zircon became colorless, indicating annealing of the radiation damage in the crystal. Two-dimensional element maps of the outermost 3 μm of unpolished zircon crystal surfaces were produced using a grind of contiguous 7 μm analytical spots via laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS). The chemical maps indicate that the surface of the zircon crystals from each experiment heterogeneously reacted with the fluid, such that the Ce and Y concentration of chemically modified areas increased (by an order of magnitude) in the CePO4-bearing and YPO4-bearing experiments, respectively, when compared with the chemical maps of unaltered zircon grain surfaces. Helium ion microscopy of polished crystals revealed discontinuous micron-scale altered domains at the crystal margin, consistent with the findings of the unpolished mapping technique. Interestingly, the Th and U concentration of the altered zircon grain surfaces were consistent with the unaltered zircon regardless of the experiment. Incorporation of REEs on the zircon grain surface likely occurred via the coupled substitution REE3+ + P5+ ↔ Zr4+ + Si4+. The results from these experiments imply that the surfaces of minimally metamict zircon can be chemically modified by alkali-bearing fluids via ion exchange under lower greenschist pressures and temperatures over relatively short time periods with respect to the geological time scale.

scholarly journals Pore Pressure Analysis for Distinguishing Earthquakes Induced by CO2 Injection from Natural Earthquakes

2020 ◽  
Vol 12 (22) ◽  
pp. 9723
Author(s):  
Chanmaly Chhun ◽  
Takeshi Tsuji
Keyword(s):  
Pore Pressure ◽  
Co2 Storage ◽  
Carbon Capture And Storage ◽  
Co2 Injection ◽  
Storage Site ◽  
Seasonal Fluctuations ◽  
Induced Earthquakes ◽  
Seismogenic Fault ◽  
Seismogenic Faults ◽  
Natural Earthquakes

It is important to distinguish between natural earthquakes and those induced by CO2 injection at carbon capture and storage sites. For example, the 2004 Mw 6.8 Chuetsu earthquake occurred close to the Nagaoka CO2 storage site during gas injection, but we could not quantify whether the earthquake was due to CO2 injection or not. Here, changes in pore pressure during CO2 injection at the Nagaoka site were simulated and compared with estimated natural seasonal fluctuations in pore pressure due to rainfall and snowmelt, as well as estimated pore pressure increases related to remote earthquakes. Changes in pore pressure due to CO2 injection were clearly distinguished from those due to rainfall and snowmelt. The simulated local increase in pore pressure at the seismogenic fault area was much less than the seasonal fluctuations related to precipitation and increases caused by remote earthquakes, and the lateral extent of pore pressure increase was insufficient to influence seismogenic faults. We also demonstrated that pore pressure changes due to distant earthquakes are capable of triggering slip on seismogenic faults. The approach we developed could be used to distinguish natural from injection-induced earthquakes and will be useful for that purpose at other CO2 sequestration sites.

scholarly journals Chemistry of Reservoir Fluids in the Aspect of CO2 Injection for Selected Oil Reservoirs in Poland

Energies ◽  
2020 ◽  
Vol 13 (23) ◽  
pp. 6456
Author(s):  
Ewa Knapik ◽  
Katarzyna Chruszcz-Lipska
Keyword(s):  
Oil Recovery ◽  
Carbon Capture ◽  
Co2 Storage ◽  
Carbon Capture And Storage ◽  
Oil Reservoirs ◽  
Co2 Injection ◽  
Oil Composition ◽  
Co2 Solubility ◽  
Geological Co2 Storage ◽  
Reservoir Conditions

Worldwide experiences related to geological CO2 storage show that the process of the injection of carbon dioxide into depleted oil reservoirs (CCS-EOR, Carbon Capture and Storage—Enhanced Oil Recovery) is highly profitable. The injection of CO2 will allow an increasing recovery factor (thus increasing CCS process profitability) and revitalize mature reservoirs, which may lead to oil spills due to pressure buildups. In Poland, such a solution has not yet been implemented in the industry. This work provides additional data for analysis of the possibility of the CCS-EOR method’s implementation for three potential clusters of Polish oil reservoirs located at a short distance one from another. The aim of the work was to examine the properties of reservoir fluids for these selected oil reservoirs in order to assure a better understanding of the physicochemical phenomena that accompany the gas injection process. The chemical composition of oils was determined by gas chromatography. All tested oils represent a medium black oil type with the density ranging from 795 to 843 g/L and the viscosity at 313 K, varying from 1.95 to 5.04 mm/s. The content of heavier components C25+ is up to 17 wt. %. CO2–oil MMP (Minimum Miscibility Pressure) was calculated in a CHEMCAD simulator using the Soave–Redlich–Kwong equation of state (SRK EoS). The oil composition was defined as a mixture of n-alkanes. Relatively low MMP values (ca. 8.3 MPa for all tested oils at 313 K) indicate a high potential of the EOR method, and make this geological CO2 storage form more attractive to the industry. For reservoir brines, the content of the main ions was experimentally measured and CO2 solubility under reservoir conditions was calculated. The reservoir brines showed a significant variation in properties with total dissolved solids contents varying from 17.5 to 378 g/L. CO2 solubility in brines depends on reservoir conditions and brine chemistry. The highest calculated CO2 solubility is 1.79 mol/kg, which suggest possible CO2 storage in aquifers.

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