Spelling suggestions: "subject:"[een] CARBON CAPTURE AND STORAGE - CCS"" "subject:"[enn] CARBON CAPTURE AND STORAGE - CCS""
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Ignition of suspensions of coal and biomass particles in air and oxy-fuel for Carbon Capture and Storage (CCS) and climate change mitigationTrabadela Robles, Ignacio January 2015 (has links)
Carbon Capture and Storage (CCS) is a legitimate technology option that should be part of a balanced portfolio of mitigation technologies available Post-Kyoto Protocol framework after Paris 2015 and beyond the 2020s or the cost achieving 2 degrees Celsius stabilisation scenario will significantly increase. Oxy-fuel combustion as a CCS technology option increases fuel flexibility. Additionally, oxy-biomass as a bio-energy with CCS (BECCS) technology can achieve negative carbon dioxide (CO2) emissions in sustainable biomass systems. Also, oxygen (O2) production in an air separation unit (ASU) gives potential for extra operational flexibility and energy storage. In this work, new designs of 20 litre spherical (R-20) and 30 litre non-spherical (R-30) ignition chambers have been built at the University of Edinburgh to carry-out dust ignition experiments with different ignition energies for evaluating pulverised fuel ignitability as a function of primary recycle (PR) O2 content for oxy-fuel PF milling safety. A set of coals and biomasses being used (at the time of submitting this work) in the utility pulverised fuel boilers in the UK have been employed. Coal and biomass dusts were ignited in air and oxy-fuel mixtures up to 30 % v/v O2 balance mixture CO2 where peak pressures (Pmax) from ignition were recorded. Pressure ratios (Pmax/Pinitial) were determined the key parameter for positive ignition identification with a value above 2.5 to be considered positive. Particle size effects in coal and biomass ignition were evaluated. Results on biomass were more variable than with coals, requiring a stronger ignition source (5,000 J) mainly due to larger particle sizes. Finer biomass particles behaved similarly to air ignition in 25 % v/v O2 in CO2. Larger particles of biomass did not ignite at all for most cases even reaching 30 % v/v O2 in CO2. A reference coal used, El Cerrejon, behaved as expected with 30 % v/v O2 balance CO2 matching air case; particles between 75-53 microns had lower ignitability than finer below 53 microns but were critical in devolatilisation. Most fuels did not ignite in 21 % v/v in CO2 below 200 g/m3 concentrations. The use of adequate ignition energy strength is needed for the PF mill safety case, with 5,000 J energy required for the biomasses tested. An indication of potential ignition chamber volume and geometry effect has also been observed when comparing results from R-20 and R-30 ignition chambers. Important implications include that oxy-biomass PR with 21 % v/v O2 content would give improved pulverised fuel (PF) milling safety when compared to air firing but reduced ignitability and a 25 % v/v O2 balance CO2 atmosphere would approach to oxy-biomass ignition behaviour in air in mills.
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Numerical modelling of geophysical monitoring techniques for CCSEid, Rami Samir January 2016 (has links)
I assess the potential of seismic and time-domain controlled-source electromagnetic (CSEM) methods to monitor carbon dioxide (CO2) migration through the application of a monitorability workflow. The monitorability workflow describes a numerical modelling approach to model variations in the synthetic time-lapse response due to CO2 migration. The workflow consists of fluid-flow modelling, rock-physics modelling and synthetic seismic or CSEM forward modelling. I model CO2 injected into a simple, homogeneous reservoir model before applying the workflow to a heterogeneous model of the Bunter Sandstone reservoir, a potential CO2 storage reservoir in the UK sector of the North Sea. The aim of this thesis is to model the ability of seismic and time-domain CSEM methods to detect CO2 plume growth, migration and evolution within a reservoir, as well as the ability to image a migrating front of CO2. The ability to image CO2 plume growth and migration within a reservoir has not been demonstrated in the field of CSEM monitoring. To address this, I conduct a feasibility study, simulating the time-lapse CSEM time-domain response of CO2 injected into a saline reservoir following the multi-transient electromagnetic (MTEM) method. The MTEM method measures the full bandwidth response. First, I model the response to a simple homogeneous 3D CO2 body, gradually increasing the width and depth of the CO2. This is an analogue to vertical and lateral CO2 migration in a reservoir. I then assess the ability of CSEM to detect CO2 plume growth and evolution within the heterogeneous Bunter Sandstone reservoir model. I demonstrate the potential to detect stored and migrating CO2 and present the synthetic results as time-lapse common-offset time sections. The CO2 plume is imaged clearly and in the right coordinates. The ability to image seismically a migrating front of CO2 remains challenging due to uncertainties regarding the pore-scale saturation distribution of fluids within the reservoir and, in turn, the most appropriate rock-physics model to simulate this: uniform or patchy saturation. I account for this by modelling both saturation models, to calculate the possible range of expected seismic velocities prior to generating and interpreting the seismic response. I demonstrate the ability of seismic methods to image CO2 plume growth and evolution in the Bunter Sandstone saline reservoir model and highlight clear differences between the two rock-physics models. I then modify the Bunter Sandstone reservoir to depict a depleted gas field by including 20% residual gas saturation. I assess the importance and implication of patchy saturation and present results which suggest that seismic techniques may be able to detect CO2 injected into depleted hydrocarbon fields.
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Carbon dioxide enhanced oil recovery, offshore North Sea : carbon accounting, residual oil zones and CO2 storage securityStewart, Robert Jamie January 2016 (has links)
Carbon dioxide enhanced oil recovery (CO2EOR) is a proven and available technology used to produce incremental oil from depleted fields. Although this technology has been used successfully onshore in North America and Europe, projects have maximised oil recovery and not CO2 storage. While the majority of onshore CO2EOR projects to date have used CO2 from natural sources, CO2EOR is now more and more being considered as a storage option for captured anthropogenic CO2. In the North Sea the lack of low cost CO2, in large volumes, has meant that no EOR projects have utilised CO2 as an injection fluid. However CO2EOR has the highest potential of all EOR techniques to maximise recovery from depleted UK oil fields. With the prospect of Carbon Capture and Storage (CCS) capturing large tonnages of CO2 from point source emission sites, the feasibility of CO2EOR deployment in the North Sea is high. This thesis primarily aims to address a number of discrete issues which assess the effectiveness of CO2EOR to both produce oil and store CO2. Given the fundamental shift in approach proposed in North Sea CO2EOR projects, the carbon balance of such projects is examined. Using a life cycle accounting approach on a theoretical North Sea field, we examine whether offshore CO2EOR can store more CO2 than onshore projects traditionally have, and whether CO2 storage can offset additional emissions produced through offshore operations and incremental oil production. Using two design scenarios which optimise oil production and CO2 storage, we find that that net GHG emissions were negative in both ‘oil optimised’ and ‘CO2 storage optimised’. However when emissions from transporting, refining and combusting the produced crude oil are incorporated into the life cycle calculations the ‘oil optimised scenario’ became a net emitter of GHG and highlights the importance of continuing CO2 import and injection after oil production has been maximised at a field. This is something that has not traditionally occurred. After assessing rates of flaring and venting of produced associated gas at UK oil fields it is found that the flaring or venting of reproduced CH4 and CO2 has a large control on emissions. Much like currently operating UK oil fields the rates of flaring and venting has a control on the carbon intensity of oil produced. Here values for the carbon intensity of oil produced through CO2EOR are presented. Carbon intensity values are found to be similar to levels of current UK oil production and significantly lower than other unconventional sources. As well as assessing the climate benefits of CO2EOR, a new assessment of CO2EOR potential in Residual Oil Zones (ROZ) is also made. ROZ resource, which is thought to add significant potential to both the oil reserves and CO2 storage potential in some US basins, is here identified in the North Sea for the first time. Based on the foundation of North Sea hydrodynamics study, this thesis identifies the Pierce field as a candidate ROZ field where hydrodynamic tilting of the oil water contact has naturally occurred leaving a zone of residual oil. To test the feasibility of CO2EOR in such a zone a methodology is presented and applied. Notably the study highlights that in this case study recoverable reserves from the ROZ may approach 20% of total field recoverable reserves and have the capability to store up to 11Mt of CO2. While highlighting the CO2EOR potential in the ROZ the thesis discusses the importance in expanding the analysis to quantify its importance on a basin scale. Discussion is also made on whether new resource identification is necessary in a mature basin like the North Sea. With CO2EOR being considered as a feasible option for storing captured anthropogenic CO2, it is important to assess the security of storage in CO2EOR. Using real geochemical and production data from a pilot CO2EOR development in Western Canada two approaches are used to assess the partitioning of CO2 between reservoir fluids through time. Using a number of correlations it is found that CO2 dissolution in oil is up to 7 times greater than in reservoir brine when saturations between the two fluids are equal. It is found that after two years of CO2 injection solubility trapping accounts for 26% of injected CO2. The finding that significantly more dissolution occurs in oil rather than brine indicates that CO2 storage in EOR is safer than in brine storage. However a number of factors such as the increase in oil/CO2 mobility due to CO2 injection is also discussed. The overall conclusion from the work is that CO2EOR in the North Sea has the potential to be an effective way of producing oil and storing CO2 in the North Sea. A number of design, operational and accounting factors are however essential to operate an exemplar CO2EOR project where low carbon intensity oil can be produced from a mature basin while storing large tonnages of captured anthropogenic CO2.
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Carbon dioxide sequestration methodothologies - A reviewMwenketishi, G., Benkreira, Hadj, Rahmanian, Nejat 30 November 2023 (has links)
Yes / The process of capturing and storing carbon dioxide (CCS) was previously considered a crucial and time-sensitive approach for diminishing CO2 emissions originating from coal, oil, and gas sectors. Its implementation was seen necessary to address the detrimental effects of CO2 on the atmosphere and the ecosystem. This recognition was achieved by previous substantial study efforts. The carbon capture and storage (CCS) cycle concludes with the final stage of CO2 storage. This stage involves primarily the adsorption of CO2 in the ocean and the injection of CO2 into subsurface reservoir formations. Additionally, the process of CO2 reactivity with minerals in the reservoir formations leads to the formation of limestone through injectivities. Carbon capture and storage (CCS) is the final phase in the CCS cycle, mostly achieved by the use of marine and underground geological sequestration methods, along with mineral carbonation techniques. The introduction of supercritical CO2 into geological formations has the potential to alter the prevailing physical and chemical characteristics of the subsurface environment. This process can lead to modifications in the pore fluid pressure, temperature conditions, chemical reactivity, and stress distribution within the reservoir rock. The objective of this study is to enhance our existing understanding of CO2 injection and storage systems, with a specific focus on CO2 storage techniques and the associated issues faced during their implementation. Additionally, this research examines strategies for mitigating important uncertainties in carbon capture and storage (CCS) practises. Carbon capture and storage (CCS) facilities can be considered as integrated systems. However, in scientific research, these storage systems are often divided based on the physical and spatial scales relevant to the investigations. Utilising the chosen system as a boundary condition is a highly effective method for segregating the physics in a diverse range of physical applications. Regrettably, the used separation technique fails to effectively depict the behaviour of the broader significant system in the context of water and gas movement within porous media. The limited efficacy of the technique in capturing the behaviour of the broader relevant system can be attributed to the intricate nature of geological subsurface systems. As a result, various carbon capture and storage (CCS) technologies have emerged, each with distinct applications, associated prices, and social and environmental implications. The results of this study have the potential to enhance comprehension regarding the selection of an appropriate carbon capture and storage (CCS) application method. Moreover, these findings can contribute to the optimisation of greenhouse gas emissions and their associated environmental consequences. By promoting process sustainability, this research can address critical challenges related to global climate change, which are currently of utmost importance to humanity. Despite the significant advancements in this technology over the past decade, various concerns and ambiguities have been highlighted. Considerable emphasis was placed on the fundamental discoveries made in practical programmes related to the storage of CO2 thus far. The study has provided evidence that despite the extensive research and implementation of several CCS technologies thus far, the process of selecting an appropriate and widely accepted CCS technology remains challenging due to considerations related to its technological feasibility, economic viability, and societal and environmental acceptance.
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A comprehensive review on carbon dioxide sequestration methodsMwenketishi, G., Benkreira, Hadj, Rahmanian, Nejat 09 December 2023 (has links)
Yes / Capturing and storing CO2 (CCS) was once regarded as a significant, urgent, and necessary option for reducing the emissions of CO2 from coal and oil and gas industries and mitigating the serious impacts of CO2 on the atmosphere and the environment. This recognition came about as a result of extensive research conducted in the past. The CCS cycle comes to a close with the last phase of CO2 storage, which is accomplished primarily by the adsorption of CO2 in the ocean and injection of CO2 subsurface reservoir formation, in addition to the formation of limestone via the process of CO2 reactivity with reservoir formation minerals through injectivities. CCS is the last stage in the carbon capture and storage (CCS) cycle and is accomplished chiefly via oceanic and subterranean geological sequestration, as well as mineral carbonation. The injection of supercritical CO2 into geological formations disrupts the sub-surface’s existing physical and chemical conditions; changes can occur in the pore fluid pressure, temperature state, chemical reactivity, and stress distribution of the reservoir rock. This paper aims at advancing our current knowledge in CO2 injection and storage systems, particularly CO2 storage methods and the challenges encountered during the implementation of each method and analyses on how key uncertainties in CCS can be reduced. CCS sites are essentially unified systems; yet, given the scientific context, these storage systems are typically split during scientific investigations based on the physics and spatial scales involved. Separating the physics by using the chosen system as a boundary condition is a strategy that works effectively for a wide variety of physical applications. Unfortunately, the separation technique does not accurately capture the behaviour of the larger important system in the case of water and gas flow in porous media. This is due to the complexity of geological subsurface systems, which prevents the approach from being able to effectively capture the behaviour of the larger relevant system. This consequently gives rise to different CCS technology with different applications, costs and social and environmental impacts. The findings of this study can help improve the ability to select a suitable CCS application method and can further improve the efficiency of greenhouse gas emissions and their environmental impact, promoting the process sustainability and helping to tackle some of the most important issues that human being is currently accounting global climate change. Though this technology has already had large-scale development for the last decade, some issues and uncertainties are identified. Special attention was focused on the basic findings achieved in CO2 storage operational projects to date. The study has demonstrated that though a number of CCS technologies have been researched and implemented to date, choosing a suitable and acceptable CCS technology is still daunting in terms of its technological application, cost effectiveness and socio-environmental acceptance.
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A novel approach to solvent screening for post-combustion carbon dioxide capture with chemical absorptionRetief, Frederik Jacobus Gideon 14 March 2012 (has links)
Thesis (MScEng)--Stellenbosch University. / ENGLISH ABSTRACT: Carbon dioxide (CO2) is classified as the main greenhouse gas (GHG) contributing to global warming.
Estimates by the Intergovernmental Panel on Climate Change (IPCC) suggest that CO2 emissions must be
reduced by between 50 to 85% by 2050 to avoid irreversible impacts. Carbon capture and storage (CCS)
strategies can be applied to de-carbonize the emissions from fossil-fueled power plants. Compared to
other CCS techniques, post-combustion capture (PCC) is most likely to be implemented effectively as a
retrofit option to existing power plants. At present however CCS is not yet commercially viable. The
main challenge with CCS is to reduce the inherent energy penalty of the CO2 separation stage on the
host plant.
Seventy-five to eighty percent of the total cost of CCS is associated with the separation stage. There are
several technologies available for separating CO2 from power plant flue gas streams. Reactive absorption
with aqueous amine solutions has the ability to treat low concentration, low pressure and large flux flue
gas streams in industrial-scale applications. It is most likely to be the first technology employed
commercially in the implementation of CCS. The energy required for solvent regeneration however, is
high for the standard solvent used in reactive absorption processes, i.e. MEA. This leads to a reduction in
thermal efficiency of the host plant of up to 15%. Alternative solvent formulations are being evaluated in
an attempt to reduce the energy intensity of the regeneration process.
The main objective of this study was to establish a novel, simplified thermodynamic method for solvent
screening. Partial solubility parameters (PSPs) were identified as the potential basis for such a method.
The major limitation of this approach is that the model doesn’t account for effects from chemical
reaction(s) between materials, e.g. CO2 reacting with aqueous alkanolamine solutions; considering only
the effects from dissolution. The EquiSolv software system was developed based on PSP theory. The
Hansen 3-set PSP approach was used to describe the equilibrium behaviour of CO2 absorbing in task
specific solvents. The Hansen theory was expanded to a 4-set approach to account for contributions
from electrostatic interactions between materials. The EquiSolv program was used successfully to screen
large sets of solvent data (up to 400 million formulations) in the search for suitable alternative solvent
formulations for CO2 absorption.
The secondary objective of this study was to evaluate the ability of the proposed PSP model to
accurately predict suitable alternative solvents for CO2 absorption through preliminary experimental
work. A series of CO2 absorption experiments were conducted to evaluate the absorption performance
of predicted alternative solvent formulations. The predicted alternative solvent formulations exhibited a
significant improvement in absorption performance (up to a 97% increase in the measured absorption
capacity) compared to conventional solvent formulations. Statistical analysis of the experimental results
has shown that there is a statistically significant concordant relationship between the predicted and
measured rankings for the absorption performance of the predicted solvent formulations. Based on this
it was concluded that PSP theory can be used to accurately predict the equilibrium behaviour of CO2
absorbing in task specific solvents.
Recently ionic liquids (ILs) have been identified as potential alternatives to alkanolamine solutions
conventionally used for CO2 absorption. Absorption experiments were conducted as a preliminary
assessment of the absorption performance of ILs. Results have shown ILs to have significantly improved
performance compared to conventional alkanolamine solvents; up to a 96% increase in the measured
absorption capacity compared to conventional solvents. Future work should focus on developing task
specific ionic liquids (TSILs) in an attempt to reduce the energy intensity of solvent regeneration in CO2
absorption processes. / AFRIKAANSE OPSOMMING: Koolsuurgas (CO2) word geklassifiseer as die vernaamste kweekhuis gas (GHG) wat bydra to globale
verwarming. Beramings deur die Interregeringspaneel oor Klimaatsverandering (IPKV) toon aan dat CO2
emissies teen 2050 verminder moet word met tussen 50 en 85% om onomkeerbare invloede te vermy.
Verskeie koolstof opvangs en bergings (KOB) strategieë kan toegepas word ten einde die koolstof
dioksied konsentrasie in die emissies van kragstasies wat fossielbrandstowwe gebruik, te verminder. Naverbranding
opvangs (NVO) is die mees aangewese KOB tegniek wat effektief toegepas kan word op
bestaande kragstasies. Tans is KOB egter nog nie kommersieël lewensvatbaarvatbaar nie. Die hoof
uitdaging wat KOB in die gesig staar is om die energie boete inherent aan die CO2 skeidingstap te
verminder.
Tussen vyf-en-sewentig en tagtig persent van die totale koste van KOB is gekoppel aan die skeidingstap.
Daar is verskeie metodes beskikbaar vir die skeiding van CO2 uit die uitlaatgasse van kragstasies.
Reaktiewe absorpsie met waterige oplossings van amiene kan gebruik word om lae konsentrasie, lae
druk en hoë vloei uitlaatgasstrome in industriële toepassings te behandel. Dit is hoogs waarskynlik die
eerste tegnologie wat kommersieël aangewend sal word in die toepassing van KOB. Die oplosmiddel wat
normalweg vir reaktiewe absorpsie gebruik word (d.w.s. MEA) benodig egter ‘n groot hoeveelheid
energie vir regenerasie. Dit lei tot ‘n afname in die termiese doeltreffendheid van die voeder aanleg van
tot 15%. Alternatiewe oplosmiddelstelsels word tans ondersoek in ‘n poging om the energie intensiteit
van die regenerasieproses te verminder.
Die hoof doelwit van hierdie studie was om ‘n nuwe, ongekompliseerde termodinamiese metode te
vestig vir die keuring van alternatiewe oplosmiddels. Parsiële oplosbaarheidsparameters (POPs) is
geïdentifiseer as ‘n moontlike grondslag vir so ‘n metode. Die model beskryf egter slegs die ontbindings
gedrag van materiale. Die effekte van chemise reaksie(s) tussen materiale, bv. die tussen CO2 en
waterige oplossings van alkanolamiene, word nie in ag geneem nie. Die POP teorie het gedien as
grondslag vir die ontwerp van die EquiSolv sagteware stelsel. Die Hansen stel van drie POPs is gebruik
om die ewewigsgedrag te beskryf van CO2 wat absorbeer in doelgerig-ontwerpte oplosmiddels. Die
Hansen teorie is verder uitgebrei na ‘n stel van vier POPs om die bydrae van elektrostatiese wisselwerking tussen materiale in ag te neem. Die EquiSolv program is verskeie kere met groot sukses
gebruik vir die sifting van groot stelle data (soveel as 400 miljoen formulasies) in die soektog na
alternatiewe oplosmiddels vir CO2 absorpsie.
Die sekondêre doelwit van die studie was om die vermoë van die voorgestelde POP model om geskikte
alternatiewe oplosmiddels vir CO2 absorpsie akkuraat te voorspel, te ondersoek deur voorlopige
eksperimentele werk. ‘n Reeks CO2 absorpsie eksperimente is gedoen ten einde die absorpsie
werkverrigting van die voorspelde alternatiewe oplosmidels te ondersoek. ‘n Verbetering in absorpsie
werkverrigting van tot 97% is gevind vir die voorspelde oplosmiddels vergeleke met die van
oplosmiddels wat tipies in die industrie gebruik word. Statistiese ontleding van die eksperimentele
resultate het getoon dat daar ‘n beduidende ooreenstemming tussen die voorspelde en gemete
rangskikking van die voorspelde oplosmiddels se werkverrigting bestaan. Dus kan POP teorie gebruik
word om die absorpsie van CO2 in doelgerig-ontwerpte oplosmiddels akkuraat te beskryf.
Ioniese vloeistowwe (IVs) is onlangs geïdentifiseer as moontlike alternatiewe oplosmidels vir die
alkanolamien oplossings wat normaalweg gebruik word vir CO2 absorpsie. Absorpsie eksperimente is
gedoen ten einde ‘n voorlopige raming van die absorpsie werkverrigting van IVs te bekom. Daar is
bevind dat IVs ‘n beduidende verbetering in werkverrigting toon in vergelyking met die alkanolamien
oplosmiddels wat normaalweg gebruik word. ‘n Verbetering in absorpsie werkverrigting van tot 96% is
gevind vir die voorspelde IV-bevattende oplosmiddels vergeleke met die van oplosmiddels wat tipies in
die industrie gebruik word. Die fokus van toekomstige navorsing moet val op die ontwikkeling van
doelgemaakte ioniese vloeistowwe (DGIVs) in ‘n poging om die energie intensiteit van oplosmiddel
regenerasie in CO2 absorpsie prosesse te verminder.
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Enhanced CO2 Storage in Confined Geologic FormationsOkwen, Roland Tenjoh 30 September 2009 (has links)
Many geoscientists endorse Carbon Capture and Storage (CCS) as a potential strategy
for mitigating emissions of greenhouse gases. Deep saline aquifers have been reported to
have larger CO
2 storage capacity than other formation types because of their availability
worldwide and less competitive usage. This work proposes an analytical model for screening
potential CO
2 storage sites and investigates injection strategies that can be employed to
enhance CO
2 storage.
The analytical model provides of estimates CO 2
storage efficiency, formation pressure
profiles, and CO 2
–brine interface location. The results from the analytical model were
compared to those from a sophisticated and reliable numerical model (TOUGH 2
). The
models showed excellent agreement when input conditions applied in both were similar.
Results from sensitivity studies indicate that the agreement between the analytical model
and TOUGH2 strongly depends on irreducible brine saturation, gravity and on the relationship
between relative permeability and brine saturation.
A series of numerical experiments have been conducted to study the pros and cons of
different injection strategies for CO 2 storage in confined saline aquifers. Vertical, horizontal,
and joint vertical and horizontal injection wells were considered. Simulations results
show that horizontal wells could be utilized to improve CO 2 storage capacity and efficiency
in confined aquifers under pressure-limited conditions with relative permeability
ratios greater than or equal to 0:01. In addition, joint wells are more efficient than single
vertical wells and less efficient than single horizontal wells for CO 2 storage in anisotropic
aquifers.
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Three essays on energy efficiency and environmental policies in CanadaGamtessa, Samuel Faye Unknown Date
No description available.
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[pt] MODELAGEM NUMÉRICA DA INJEÇÃO DE CO2 EM AQUÍFERO SALINO, OBJETIVANDO AVALIAR O APRISIONAMENTO MINERAL / [en] NUMERICAL MODELING OF CO2 INJECTION IN SALINE AQUIFERS, AIMING TO EVALUATE MINERAL STORAGEROBERTA DOMINGOS RODRIGUES 13 December 2017 (has links)
[pt] Para contribuir com a mitigação das mudanças climáticas, tecnologias com o intuito de promover a redução de emissões dos Gases de Efeito Estufa, como é o caso do dióxido de carbono, tem obtido grande destaque nas pesquisas ultimamente. Uma das alternativas para impedir que todo esse carbono seja liberado para a
atmosfera é reinjetar o CO2 nos próprios reservatórios ou em outras formações geológicas próximas. Neste sentido, esta dissertação apresenta uma tecnologia relacionada à captura e armazenamento geológico de CO2 e avalia o processo de injeção de dióxido de carbono em aquíferos salinos. O principal objetivo é avaliar o processo de injeção de dióxido de carbono em aquíferos salinos de rochas carbonáticas, numa escala de tempo de três mil anos, para avaliar o aprisionamento do CO2 em suas diferentes formas, incluindo o armazenamento mineral. Tal estudo também considera na modelagem, as reações químicas entre os componentes na fase aquosa e a difusão molecular do dióxido de carbono na fase aquosa, assim como as reações químicas de dissolução e precipitação mineral. A partir das informações obtidas em literatura, estabeleceu-se as premissas para a simulação do caso base, e gerou-se casos derivados variando individualmente cada uma das seguintes propriedades: difusividade, salinidade, pH e temperatura, no qual avaliou-se a contribuição de cada uma delas nas diferentes formas de armazenamento do CO2. Por fim, concluiu-se que a mineralização do CO2 iniciou-se após aproximadamente 200 anos de simulação. No entanto, devido às lentas taxas da reação de precipitação mineral, a predominância do armazenamento do CO2 ainda foi na forma dissolvida. As propriedades variadas que contribuíram para o aumento do armazenamento mineral de CO2, que é considerada a forma mais estável, foram: menor fator de difusividade, maior salinidade do aquífero, pH básico (pH igual a 8,0) e
maior temperatura. / [en] In order to contribute to climatic changes mitigation, technologies aiming the reduction of pollution gases emissions, such as carbon dioxide, have been highlighted in recent researches. One of the alternatives to prevent all this carbon from being released into the atmosphere is to reinject CO2 into reservoirs or in other nearby geological formations. In this sense, this work presents a technology related to the capture and geological storage of CO2 and evaluates the carbon dioxide injection process into saline aquifers. The main objective is to evaluate the carbon dioxide injection process in saline aquifers of carbonate rocks, in a time scale of three thousand years, to evaluate the storage mechanism of CO2 in its different
forms, including mineral storage. Such study also considers in the modeling, the chemical reactions between the components in the aqueous phase and the molecular diffusion of the carbon dioxide in the aqueous phase, as well as the chemical reactions of mineral dissolution and precipitation. From the research made and the information gathered in the literature, the premises for the simulation of the base case were established, and derivative cases were generated by individually varying each of the following properties: diffusivity, salinity, pH and temperature, in which the contribution of each property was evaluated on the different CO2 storage forms. Finally, it was concluded that the injected CO2 mineralization process started after approximately 200 years of simulation. However, due to slow rates of the mineral precipitation, the CO2 storage in the dissolved form was still predominant. The different properties that contributed to increase the CO2 mineral storage, which is considered the more estable one, were: lower diffusivity factor, higher aquifer salinity, basic pH (pH equal to 8.0) and higher temperature.
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[pt] MODELAGEM NUMÉRICA DA INJEÇÃO ALTERNADA DE ÁGUA E GÁS INTEGRADA À GEOQUÍMICA DE RESERVATÓRIO / [en] NUMERICAL MODELING OF WATER ALTERNATING GAS INJECTION INCOPORATING RESERVOIR GEOCHEMISTRYRITA DE CASSIA ARAGAO DE OLIVEIRA 01 February 2022 (has links)
[pt] Como solução para viabilizar a produção de óleo com alto teor de dióxido
de carbono, condição característica do pré-sal brasileiro, foi escolhida a estratégia
de reinjeção desse mesmo gás produzido como método de recuperação de
petróleo e como instrumento de mitigação da emissão atmosférica desse tipo de
GEE (Gas do Efeito Estufa). A combinação de duas técnicas de recuperação, a
injeção de água e a de gás, conhecida como WAG (Water Alternated Gas) se
mostrou promissora por combinar benefícios como a varredura microscópica do
gás com a estabilidade e economia obtidas pela injeção de água. Este projeto tem
como objetivo entender o potencial de produção para traçar uma estratégia de
otimização de recuperação do óleo aliado ao armazenamento da maior
quantidade de CO2 possível, por meio de simulações numéricas de fluxo contínuo
por modelos composicionais. A metodologia adotada para este projeto foi a
utilização de módulos comerciais de simulação de reservatórios, fornecidos pela
CMG (Computer Modeling Group), para ajuste de dados PVT de um fluido com
características próximas ao do pré-sal, para que este pudesse ser aplicado em
dois modelos sintéticos de reservatórios, para otimização de campo e avaliação
deste pós período de produção. Desta forma, o presente trabalho proporciona uma
visão do comportamento do método WAG e sua influência sobre o fator de
recuperação deste reservatório, além de discutir as interações envolvidas em
microescala em um ambiente reativo como um reservatório carbonático na
presença do CO2. A partir dos resultados obtidos com a simulação, é possível
concluir que as reações químicas entre os componentes aquosos e minerais
presentes na formação porosa tem como consequência o aprisionamento do
carbono. / [en] The strategy of CO2 produced reinjection is a solution to enable the pre-salt
oil production as a petroleum recovery method and as an instrument to
mitigate atmospheric emission of this GHG (Greenhouse Gas). The
combination of two recovery techniques, water and gas injection, is known
as Water Alternated Gas (WAG) has shown a successful combination of
benefits such as microscopic gas sweeping with the stability and economy
achieved by water injection. This project aims to understand the production
potential to outline an optimization strategy of oil recovery coupled with the
CO2 maximum storage possible, through numerical simulations of
continuous flow by compositional models. The methodology adopted for
this project was the use of commercial reservoir simulation modules,
provided by CMG (Computer Modeling Group), to adjust PVT data of a fluid
with similar characteristics to the pre-salt oil and then it could be applied in
two synthetic reservoir models for field optimization and evaluation of this
postproduction period. Thus, the present work provides an insight into the
behavior of the WAG method and its influence on the recovery factor of this
reservoir as well as discussing the microscale interactions involved in a
reactive environment as a carbonate reservoir in the presence of CO2.
Findings obtained by the simulation process shows that the chemical
reactions between the aqueous and mineral components present in the
porous formation result in carbon entrapment.
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