La capture du CO2 en sortie d’une centrale thermique constitue un réel défi technologique. Les procédés d’adsorption peuvent être utilisés pour traiter de telles fumées caractérisées principalement par leurs grands débits et leurs faibles teneurs en CO2 (2x106 à 3x106 m3.h-1 pour une centrale de 750 MW, % Vol de CO2 = 12-15 %). Certains procédés d’adsorption existants comme les procédés PSA et TSA ont été utilisés pour le traitement des COV. Dans le cas de l’adsorption modulée en pression (PSA) l’effluent à traiter passe à travers d’un lit fixe d’adsorbant à haute pression. L’adsorbant est régénéré en baissant la pression. Pour l’adsorption modulée en température (TSA), l’adsorbant est régénéré en augmentant sa température. C’est souvent de l’air chaud qui est utilisé pour chauffer le lit. Ces deux procédés ne semblent pas bien adaptés pour la capture du CO2. Alors que le premier nécessite l’augmentation de la pression de grands débits de gaz, le deuxième procédé, basé sur le chauffage avec de l’air chaud, n’est pas énergétiquement efficace. De plus le CO2 récupéré est dilué par de l’air. L’objectif de ce travail est d’étudier un nouveau procédé d’adsorption qui permet de : 1- Traiter de grands débits de gaz à faible pression et capturer la majeure partie du dioxyde de carbone qu’ils contiennent ; 2- Récupérer le CO2 avec une haute pureté ; 3- Réduire le coût énergétique de la régénération. Pour réaliser ce travail, trois procédés d’adsorption ont été examinés expérimentalement et théoriquement : Adsorption avec régénération électrothermique (ESA), Adsorption avec régénération sous vide (VSA) et ESA-VSA couplés. La première étape du travail a consisté à choisir un adsorbant performant. Pour cela, plusieurs solides ont été considérés (charbons actifs, tamis moléculaires carbonés, matériaux polymères, zéolites ...) et deux adsorbants ont été choisis (zéolite 5A et matériau composite PDMS-charbon actif). Dans le cas de la régénération électrothermique, l'adsorbant a été chauffé de façon indirecte, par l'effet de Joule. Après avoir étudié les trois méthodes de régénération expérimentalement, un module de calcul a été développé au moyen de COMSOL la Multiphysics permettant d'ajuster les paramètres de cinétique de transfert de masse pour les étapes d'adsorption et de régénération / The recovery of CO2 from the fossil fuel power plant flue gas is a very important technical challenge. Adsorption processes can be applied to recover CO2 from such dilute and voluminous flue gas (2x106 to 3x106 m3.h-1 for a 750 MW power plant, CO2 Vol % = 12-15 %). Some existing processes like PSA and TSA have been used for VOCs separation. In pressure Swing Adsorption (PSA) the gas mixture flows through a packed bed of adsorbent at elevated pressure. The bed is regenerated by reducing the pressure. In Temperature Swing Adsorption (TSA), the bed is regenerated by raising its temperature. It is generally based on air heating. These two processes do not seem adapted for CO2 recovery. The first one needs an increase of a very voluminous flue gas pressure. TSA based on air heating is not energitically efficient and it produces diluted CO2. In this work, we aim to study a new adsorption process that permitts to: 1- treat voluminous flue gas at low pressure to recover most of the carbon dioxide that it contains 2- recover CO2 with a high purity 3- reduce the energitic cost of the regeneration To do this work, three adsorption processes were examined experimentally and theoretically: Electrothermal Swing Adsorption (ESA), Vaccum Swing Adsorption (VSA) and coupled ESA-VSA. The first step of the work consisted in the choice of a performent adsorbent. Thus different solids were tested (active carbon, carbon molecular sieves, polymer adsorbents, zeolites...) and two adsorbents which were chosen (zeolite 5A and mixed matrix PDMS-active carbon). For the electrothermal regeneration, the adsorbents were heated indirectly by Joule effect. After having tested the three different ways of regeneration experimentally, different calculation modules were created using COMSOL Multiphysics, permitting adjust the kinetic and mass transfer parameters for both adsorption and regeneration

CCS, Carbon Capture and Storage, innebär infångning och lagring av koldioxid från stora punktutsläpp. Detta gör cementindustrin aktuell för implementering av CCS. Stora delar av branschens koldioxidutsläpp går inte att eliminera på annat sätt. Kostnaden för monoetanolamin-baserad post-combustion capture med efterföljande transport och lagring av koldioxiden vid cementfabriken Cementa AB i Degerhamn undersöktes. Studiens kostnadsberäkningar är baserade på publicerade uppgifter om kostnaden för koldioxidinfångning vid den norska cementfabriken Norcem Brevik, och på publicerade uppgifter om kostnaden för transport av koldioxid till en lagringsplats i Östersjön. Cementa Degerhamns koldioxidutsläpp kan reduceras med 5,4 miljoner ton under en 25-årsperiod till en kostnad av 2,2 miljarder SEK. Slutresultatet, som uttrycks i måttet Cost of CO2 avoided, ger en kostnad på 890 SEK/ton CO2. En känslighetsanalys visar att av de undersökta parametrarna är storleken på koldioxidutsläppen och kostnaden för användning och underhåll viktigast för storleken på Cost of CO2 avoided. Vidare studier behövs för en mer exakt beräkning av kostnaden för CCS vid Cementa Degerhamn. / CCS, Carbon Capture and Storage, involves the capture and storage of carbon dioxide from large point sources. This makes the cement industry suitable for the implementation of CCS. Large parts of the industry's carbon dioxide emissions cannot be eliminated by other means. The cost of monoethanolamine-based post-combustion capture and subsequent transport and storage of the carbon dioxide at the cement factory Cementa AB in Degerhamn was studied. This study's cost estimates are based on published data on the cost of carbon capture at the Norwegian cement plant Norcem Brevik, and on published data on the cost of transport of carbon dioxide to a storage site in the Baltic Sea. Cementa Degerhamn’s carbon dioxide emissions can be reduced by 5.4 million tons over a 25 year period to a cost of 2.2 billion SEK. The result, expressed in Cost of CO2 avoided, gives a cost of 890 SEK/ton CO2. A sensitivity analysis shows that of the examined parameters, the size of the carbon dioxide emissions and the cost of use and maintenance are the most important for the size of Cost of CO2 avoided. Further studies are required for a more accurate calculation of the cost of CCS at Cementa Degerhamn.

Dispatchable low carbon electricity has been identified as a key requirement for low carbon electricity systems because these systems must provide reliable electricity services to an increasing portion of the world’s population while utilising an increasing share of nondispatchable assets such as renewable and nuclear generators. Fossil fuel generators can provide dispatchable low carbon electricity by leveraging post-combustion carbon capture technologies assuming post-combustion capture (PCC) plants can operate in a flexible and efficient manner. This thesis explores the connection between solvent analysis techniques and the optimal operation of PCC plants with a particular focus on process optimisation and control under flexible and transient conditions. The connection between solvent analysis measurements and PCC plant process control and optimisation strategies is established. An ideal set of analysis technique criteria is established for flexible post-combustion capture plants. Currently available solvent analysis techniques are surveyed and evaluated against the ideal set of criteria. Specific weaknesses of current techniques are highlighted and two novel solvent analysis techniques are introduced to address these weaknesses. The first provides continuous amine concentration and CO2 loading measurements at process flow conditions by inferring solvent chemical composition from physical properties. This method was evaluated by deploying an instrument prototype to a post-combustion pilot plant to continuously analyse solvent during a test campaign which simulated flexible plant operation. The measurement results were compared against industry standard solvent analysis techniques and the inferential technique was found to produce sufficient measurement accuracy and sensitivity while providing a faster, lower cost and more robust measurement technique. The second technique combines the strengths of several currently available CO2 loading techniques to measure CO2 gas evolved from an acidified solvent under vacuum conditions. The technique was found to provide superior measurement accuracy and sensitivity compared to currently available methods when measuring lab standard solutions. The integration of these novel analysis techniques into advanced process control systems is proposed and future method improvements are suggested.

Carbon dioxide CO₂capture through hydrate formation is a novel technology under consideration as an efficient means of separating CO₂from flue/fuel gas mixtures for sequestration and enhanced oil recovery operations. This thesis examines post-combustion capture of CO₂from fossil-fuel power plant flue-gas streams through hydrate formation in a silica gel column. Power plant flue-gas contains essentially CO₂and nitrogen (N2) after suitable pre-treatment steps, thus a model flue-gas comprising 17% co₂and 83% N2 was used in the study. Previous studies employed a stirred-tank reactor to achieve water-gas contact for formation of hydrates; recent microscopic studies involved using water dispersed in silica gel to react with gas, showing potential for improved hydrate formation rates without the need for agitation. This study focuses on macroscopic kinetics of hydrate formation in silica gel to evaluate hydrate formation rates, CO₂separation efficiency and determining optimal silica gel properties as a basis for a CO2 capture process. Spherical silica gels with 30.0 and 100.0 nm pore sizes and 40-75 and 75-200 μm particle sizes were studied to determine pore size and particle size effects on hydrate formation. 100.0 nm pores achieved higher gas uptake and CO₂recovery over the 30.0 nm case. Improved CO₂separation was obtained when 75-200 μm particles with 100.0 nm pores were used. The two effects observed are due to improved gas diffusion occurring with larger pore and particle size, favouring increased hydrate formation. Compared to stirred-tank experiments, results in this study show a near four-fold increase in moles of gas incorporated in the hydrate per mole of water, showing that improved water-to-hydrate conversion is obtained with pore-dispersed water. At similar experimental conditions, CO₂recovery improved from 42% for stirred-tank studies to 51% for the optimum silica (100.0 nm 75-200 μm) determined in this study. Finally, effects of tetrahydrofuran (THF) - an additive that reduces operating pressure were evaluated. Experiments with 1 mol% THF, the optimum determined from previous stirred tank studies, showed improved gas consumption in silica but reduced CO₂recovery, indicating that the optimum concentration for use in silica is different from that in stirred-tank experiments.

Carbon dioxide CO₂capture through hydrate formation is a novel technology under consideration as an efficient means of separating CO₂from flue/fuel gas mixtures for sequestration and enhanced oil recovery operations. This thesis examines post-combustion capture of CO₂from fossil-fuel power plant flue-gas streams through hydrate formation in a silica gel column. Power plant flue-gas contains essentially CO₂and nitrogen (N2) after suitable pre-treatment steps, thus a model flue-gas comprising 17% co₂and 83% N2 was used in the study. Previous studies employed a stirred-tank reactor to achieve water-gas contact for formation of hydrates; recent microscopic studies involved using water dispersed in silica gel to react with gas, showing potential for improved hydrate formation rates without the need for agitation. This study focuses on macroscopic kinetics of hydrate formation in silica gel to evaluate hydrate formation rates, CO₂separation efficiency and determining optimal silica gel properties as a basis for a CO2 capture process. Spherical silica gels with 30.0 and 100.0 nm pore sizes and 40-75 and 75-200 μm particle sizes were studied to determine pore size and particle size effects on hydrate formation. 100.0 nm pores achieved higher gas uptake and CO₂recovery over the 30.0 nm case. Improved CO₂separation was obtained when 75-200 μm particles with 100.0 nm pores were used. The two effects observed are due to improved gas diffusion occurring with larger pore and particle size, favouring increased hydrate formation. Compared to stirred-tank experiments, results in this study show a near four-fold increase in moles of gas incorporated in the hydrate per mole of water, showing that improved water-to-hydrate conversion is obtained with pore-dispersed water. At similar experimental conditions, CO₂recovery improved from 42% for stirred-tank studies to 51% for the optimum silica (100.0 nm 75-200 μm) determined in this study. Finally, effects of tetrahydrofuran (THF) - an additive that reduces operating pressure were evaluated. Experiments with 1 mol% THF, the optimum determined from previous stirred tank studies, showed improved gas consumption in silica but reduced CO₂recovery, indicating that the optimum concentration for use in silica is different from that in stirred-tank experiments.

Carbon dioxide CO₂capture through hydrate formation is a novel technology under consideration as an efficient means of separating CO₂from flue/fuel gas mixtures for sequestration and enhanced oil recovery operations. This thesis examines post-combustion capture of CO₂from fossil-fuel power plant flue-gas streams through hydrate formation in a silica gel column. Power plant flue-gas contains essentially CO₂and nitrogen (N2) after suitable pre-treatment steps, thus a model flue-gas comprising 17% co₂and 83% N2 was used in the study. Previous studies employed a stirred-tank reactor to achieve water-gas contact for formation of hydrates; recent microscopic studies involved using water dispersed in silica gel to react with gas, showing potential for improved hydrate formation rates without the need for agitation. This study focuses on macroscopic kinetics of hydrate formation in silica gel to evaluate hydrate formation rates, CO₂separation efficiency and determining optimal silica gel properties as a basis for a CO2 capture process. Spherical silica gels with 30.0 and 100.0 nm pore sizes and 40-75 and 75-200 μm particle sizes were studied to determine pore size and particle size effects on hydrate formation. 100.0 nm pores achieved higher gas uptake and CO₂recovery over the 30.0 nm case. Improved CO₂separation was obtained when 75-200 μm particles with 100.0 nm pores were used. The two effects observed are due to improved gas diffusion occurring with larger pore and particle size, favouring increased hydrate formation. Compared to stirred-tank experiments, results in this study show a near four-fold increase in moles of gas incorporated in the hydrate per mole of water, showing that improved water-to-hydrate conversion is obtained with pore-dispersed water. At similar experimental conditions, CO₂recovery improved from 42% for stirred-tank studies to 51% for the optimum silica (100.0 nm 75-200 μm) determined in this study. Finally, effects of tetrahydrofuran (THF) - an additive that reduces operating pressure were evaluated. Experiments with 1 mol% THF, the optimum determined from previous stirred tank studies, showed improved gas consumption in silica but reduced CO₂recovery, indicating that the optimum concentration for use in silica is different from that in stirred-tank experiments. / Applied Science, Faculty of / Chemical and Biological Engineering, Department of / Graduate

Carbon dioxide (CO2) has long been regarded as the major greenhouse gas, which leads to numerous negative effects on global environment. The capture and separation of CO2 by selective adsorption using porous materials proves to be an effective way to reduce the emission of CO2 to atmosphere. Porous organic polymers (POPs) are promising candidates for this application due to their readily tunable textual properties and surface functionalities. The objective of this thesis work is to develop new POPs with high CO2 adsorption capacities and CO2/N2 selectivities for post-combustion effluent (e.g. flue gas) treatment. We will also exploit the correlation between the CO2 capture performance of POPs and their textual properties/functionalities. Chapters Two focuses on the study of a group of porous phenolic-aldehyde polymers (PPAPs) synthesized by a catalyst-free method, the CO2 capture capacities of these PPAPs exceed 2.0 mmol/g at 298 K and 1 bar, while keeping CO2/N2 selectivity of more than 30 at the same time. Chapter Three reports the gas adsorption results of different hyper-cross-linked polymers (HCPs), which indicate that heterocyclo aromatic monomers can greatly enhance polymers’ CO2/N2 selectivities, and the N-H bond is proved to the active CO2 adsorption center in the N-contained (e.g. pyrrole) HCPs, which possess the highest selectivities of more than 40 at 273 K when compared with other HCPs. Chapter Four emphasizes on the chemical modification of a new designed polymer of intrinsic microporosity (PIM) with high CO2/N2 selectivity (50 at 273 K), whose experimental repeatability and chemical stability prove excellent. In Chapter Five, we demonstrate an improvement of both CO2 capture capacity and CO2/N2 selectivity by doping alkali metal ions into azo-polymers, which leads a promising method to the design of new porous organic polymers.

The purpose of the current study is to increase the understanding of different steelmaking processes at the decarburization stages by use of mathematical modeling. More specifically, two De-Laval nozzles from a VOD (Vaccum Oxygen Decarburization) process, which is used for producing stainless steels with ultra-low carbon grades, was investigated for different vessel pressures. Moreover, the post combustion phenomena in a BOF or LD (Linz-Donawitz) process as well as an AOD (Argon Oxygen Decarburization) process were studied focusing on the decarburization stage. Two industrial VOD nozzles were numerically studied and compared at different temperatures and ambient pressures. Flow patterns of the oxygen jet under different ambient pressures were predicted and the flow information at different positions from the nozzle was analyzed. In addition, the effects of different ambient temperatures on the jet velocity and the dynamic pressure were compared. The predictions revealed that a little under-expansion is somewhat helpful to improve the dynamic pressure. The jet dynamic pressure and its width for the specific nozzle geometry were also studied. It was observed that a variation in the ambient pressure can influence the jet momentum and its width. In addition, a high ambient temperature was found to have a positive effect on the improvement of the jet dynamic pressure. Furthermore, it was found that a change in ambient pressure has a stronger effect on the jet force than a change in the ambient temperature. In addition, it was proved that the profiles of the dynamic pressure at a certain blowing distance fit well to Multi-Gaussian distribution. Post combustion in a BOF/LD and an AOD process during decarburization was also studied. Two mathematical models were created to show the post combustion phenomenon inside the converters, respectively. For the CFD modeling of the two processes, the realizable k-ɛ model, the species transport model and the discrete ordinate were adopted to calculate the turbulence, gas reaction and radiation present in the gas phase in the converter. For the BOF/LD modeling, a series of plant tests were conducted to collect data, which were used in the current model. These include the off-gas information, emissivity data, oxygen blowing parameters and the chemical composition of steel. After the simulation, the predicted flow pattern and detailed information of the gases taking part in the post combustion were compared to plant data. Specifically, the off-gas data from the plant was used for the model verification. The measured CO2 concentration was 15-20 wt% and the predicted value from the modeling was 16.7 wt%. For the AOD converter of interest in the current work, a fan is installed in the end of the AOD flue to help extract the off-gas from the converter. The influence of different fan gauge pressures as well as temperatures of the gas mixture, containing the generated CO and argon, on the post combustion in the whole AOD system was studied. It was indicated from the modeling results that the post combustion was only present in the flue for the present modeling conditions. Moreover, a critical fan gauge pressure (approx.. -550 Pa) was found which could yield a maximum post combustion in the flue gas. For both two models (BOF/LD and AOD), simulations indicated that a change of the converter temperature from 1500 to 1700 °C did not influence the post combustion reaction to a large degree. In addition, these two models can be regarded as the first step for a future more in-depth modeling work of the post combustion. / <p>QC 20130913</p>

With an increased urgency for global action towards climate change mitigation, this research was undertaken with the aim of evaluating post-combustion CO2 capture as an emission abatement strategy for gas-fired power plants. A dynamic rate-based model of a capture plant with MEA solvent was built, with imposed chemical equilibrium, and validated at pilot scale under transient conditions. The model predicted plant behaviour under multiple process inputs and disturbances. The validated model was next used to analyse the process and it was found that CO2 absorption is mass transfer limited. The model was then improved by explicitly adding reactions rate in the model continuity, the first such dynamic model to be reported for the capture process. The model is again validated and is observed to provide better predictions than the previous model. Next, high fidelity models of a gas-fired power plant, a scaled-up capture plant and a compression train were built and integrated for 90% CO2 capture. Steam for solvent regeneration is extracted from the power plant IP/LP crossover pipe. Net efficiency drops from 59% to 49%, with increased cooling water demand. A 40% exhaust gas recirculation resulted in a recovery of 1% efficiency, proving that enhanced mass transfer in the capture plant reduces solvent regeneration energy demands. Economic analysis reveals that overnight cost increases by 58% with CO2 capture, and cost of electricity by 30%. While this discourages deployment of capture technology, natural gas prices remain the largest driver for cost of electricity. Other integration approaches – using a dedicated boiler and steam extraction from the LP steam drum – were explored for operational flexibility, and their net efficiencies were found to be 40 and 45% respectively. Supplementary firing of exhaust gas may be a viable option for retrofit, as it is shown to minimise integrated plant output losses at a net efficiency of 43.5%. Areas identified for further study are solvent substitution, integrated plant part load operation, flexible control and use of rotating packed beds for CO2 capture.

Le but principal de ce projet doctoral est de déterminer le potentiel d'amélioration de l'efficacité énergétique du système de captage de carbone dans les stations thermiques de production d'électricité, par l'intégration optimale des éjecteurs monophasiques. Il s'agit du système de captage postcombustion du dioxyde de carbone (CO2) par absorption/désorption utilisant la monoéthanolamine (MEA). Les éjecteurs intégrés utilisent des rejets thermiques de 100 °C qu'on retrouve dans les stations thermiques de production d'électricité. La revalorisation de ces rejets permet la substitution partielle de vapeur de turbine à coût élevé, qui serait autrement prise de la centrale thermique. Le deuxième objectif de la thèse est d'évaluer expérimentalement la performance d'un éjecteur à vapeur où le fluide secondaire de l'éjecteur est un mélange de vapeur d'eau et d'un gaz non-condensable, dans le cas présent, le CO2. Deux tuyères d'éjecteur à vapeur, d'un diamètre de 4.60 mm et 4.23 mm, ont été évaluées sur une plage de niveaux de CO2 dans le fluide secondaire, jusqu'à environ 40% en masse. La pression primaire était maintenue à 450 kPa avec une surchauffe à 10 °C et la pression secondaire était de 70 kPa. On a constaté que la pression critique ne changeait pas à mesure que la fraction massique de CO2 dans le fluide secondaire augmentait. Cependant, le rapport d'entraînement a augmenté de façon linéaire sur la plage expérimentale. Une amélioration de 23% du rapport d'entraînement par rapport à la vapeur pure a été observée lorsque le fluide secondaire contient 42% de CO2 par masse. Ce comportement contraste nettement avec le comportement observé expérimentalement d'un éjecteur à vapeur pure, où une augmentation du rapport d'entraînement se produit au détriment d'une diminution de la pression critique. Trois articles détaillés ont été publiés sur divers scénarios d'intégration d'un éjecteur à vapeur dans un procédé de captage d'absorption/désorption. Le solvant de référence était de 20% en masse de monoéthanolamine (MEA). Trois configurations principales ont été étudiées, selon le choix du fluide utilisé pour produire la vapeur secondaire : éjecteur sur condensat, éjecteur sur pauvre ou éjecteur sur riche. La première publication de revue scientifique a porté sur le procédé de désorption et a présenté une méthode de raccourci basée sur les propriétés du mélange CO2-MEA-H2O à l'équilibre. Les simulations ont révélé des réductions dans la quantité requise d'énergie de haute qualité, de 10 à 25%. Un simulateur de procédé commercial, Aspen Plus, a été utilisé pour les deux autres publications. Dans la deuxième publication de revue scientifique, le module cinétique rate-based a été utilisé, au lieu du module d'équilibre, pour la modélisation de l'absorbeur et du désorbeur, permettant des évaluations énergétiques plus près des valeurs qu'on retrouve dans la littérature courante. Une étude a été réalisée pour comparer un scénario de préchauffage de la vapeur primaire par des rejets thermiques externes avec un scénario d'intégration de la chaleur interne. Cette deuxième publication a montré des économies d'énergie de haute qualité, de 10 à 14%, les scénarios avantageux ayant été «éjecteur sur condensat» et «éjecteur sur pauvre». / Abstract : The main goal of the doctoral project is to determine to what extent the optimal integration of single-phase ejectors might reduce the large amount of energy required to capture carbon dioxide from electric power generation facilities. More specifically, the objective is to determine if ejectors can be advantageously integrated into a post-combustion absorption/desorption carbon dioxide (CO2) capture process using monoethanolamine (MEA). The integrated ejectors will use waste heat of 100 °C from the electric power plant. The upgraded waste heat can partially replace valuable turbine steam that would otherwise be taken from the power plant. The second objective of the thesis is to experimentally evaluate the performance of a steam ejector where the ejector secondary fluid is a mixture of steam and a non-condensable gas, in this case CO2. Two steam ejector nozzles, of 4.60 mm and 4.23 mm diameter, were evaluated over a range of secondary fluid CO2 levels, up to 42% by mass. The primary pressure was maintained at 450 kPa with 10 °C superheat and the secondary pressure was 70 kPa. It was found that the critical exit pressure did not change as the mass fraction of CO2 in the secondary fluid increased. The entrainment ratio, however, increased approximately linearly over the experimental range. An improvement of 23% in the entrainment ratio, as compared with pure steam, was found when the secondary fluid contains 42% CO2 by mass. This behaviour is in sharp contrast to the experimentally observed behaviour of a pure steam ejector, where an increase in entrainment ratio comes at the expense of a decrease in the ejector exit critical pressure. Three published papers investigated various scenarios for the integration of a steam injector into an absorption/desorption post-combustion capture process. The reference solvent was 20% weight monoethanolamine (MEA). Three principal configurations were studied, according to the choice for the liquid flow used to produce the ejector secondary steam: ejector on condensate, ejector on lean or ejector on rich. The first journal publication focused on the desorption process and presented a shortcut method based on CO2-MEA-H2O equilibrium vapour liquid data. The simulations revealed reductions in the required amount of valuable energy from 10 to 25%. A commercial process simulator, Aspen Plus, was used for two other publications. In the second journal publication, the kinetic rate-based module was employed to model the absorber and desorber, providing energy evaluations closer to values in the open literature. A study was included comparing preheating the primary steam with waste heat or by heat integration. The rate-based simulation found valuable energy savings of 10 to 14%, with the "ejector on condensate" and "ejector on lean" again being the advantageous scenarios.