Modeling CO2 absorption into concentrated aqueous monoethanolamine and piperazine

Dugas and Rochelle (2011) measured CO₂ mass transfer rates in 7–13 molal aqueous monoethanolamine (MEA) and 2–12 molal piperazine (PZ) from 40 to 100 °C over a large range of CO₂ loading. They observed that the liquid phase mass transfer coefficient (k′_g) was almost independent of amine concentration and temperature. In this paper models are created to explain this behavior.CO₂ reaction rates in MEA and PZ are represented with termolecular (base catalysis) kinetics with activity-based rate expressions. Solving the activity-based rate expressions with a shell balance and implementing diffusion resistance using film theory yielded an expression for the liquid phase mass transfer coefficient, k′_g. Parameters in the k′_g expression were estimated from existing literature data. Two pre-exponential rate constants (k_MEA and k_PZ) are the only parameters that were adjusted to match experimental data.Estimates from independent sources of parameters in the model for k′_g fully account for the observed effects of CO₂ loading, temperature, and amine concentration. The k′_g expressions match the 93 wetted wall column experimental rates measured by Dugas and Rochelle (2011) with average deviations of 13% for MEA and 19% for PZ. The mass transfer expressions also match experimental data obtained by other researchers.This model shows that complex rate behavior in MEA and PZ systems can be fully explained using existing literature data. It also shows that the MEA and PZ systems can be represented by termolecular kinetics on an activity basis.     

Mathematical modelling of mass-transfer and hydrodynamics in CO2 absorbers packed with structured packings

This paper presents a mechanistic model that can predict mass-transfer performance and provide an insight into dynamic behavior within structured packings used for CO₂ absorption. The model was built upon the kinetics and thermodynamics of the absorption system, as well as the liquid irrigation features and the geometry of packing elements. A computer program (Fortran 90) was written to simulate CO₂ absorption into aqueous solutions of sodium hydroxide (NaOH) and monoethanolamine (MEA) in a column packed with Gempak 4A, Mellapak 500Y and Mellapak 500X. The simulation gave essential information, including the concentration of CO₂ in gas-phase, concentration of reactive species in the liquid-phase, system temperature, mass-transfer coefficients (k_G and k_L), and effective interfacial area (a_e) for mass-transfer at different axial positions along the absorption column. The simulation also provided liquid distribution plots representing the quality of liquid distribution or maldistribution across the cross-section of the column. Verification of the model was achieved by comparing simulation results with experimental data. Very good agreement was found for wide ranges of operating and design parameters, including liquid load and initial liquid distribution pattern.     

Thermodynamic modeling of CO2 solubility in aqueous solutions of NaCl and Na2SO4

A thermodynamic model based on the electrolyte NRTL activity coefficient equation and PC-SAFT equation-of-state is developed for CO₂ solubility in aqueous solutions of NaCl and Na₂SO₄ with temperature up to 473.15 K, pressure up to 150 MPa, and salt concentrations up to saturation. The Henry's constant parameters of CO₂ in H₂O and the characteristic volume parameters for CO₂ required for pressure correction of Henry's constant are identified from fitting the experimental gas solubility of CO₂ in pure water with temperature up to 473.15 K and pressure up to 150 MPa. The NRTL binary parameters for the CO₂-(Na⁺, Cl⁻) pair and the CO₂-(Na⁺, SO₄²⁻) pair are regressed against the experimental VLE data for the CO₂-NaCl-H₂O ternary system up to 373.15 K and 20 MPa and the CO₂-Na₂SO₄-H₂O ternary system up to 433.15 K and 13 MPa, respectively. Model calculations on solubility and heat of solution of CO₂ in pure water and aqueous solutions of NaCl and Na₂SO₄ are compared to the available experimental data of the CO₂-H₂O binary, CO₂-NaCl-H₂O ternary and CO₂-Na₂SO₄-H₂O ternary systems with excellent results.     

Simulation of SO2 absorption into sulfuric acid solutions containing hydrogen peroxide in the fast and moderately fast kinetic regimes

Absorption of sulfur dioxide into aqueous solutions containing hydrogen peroxide results in the irreversible oxidation to sulfuric acid. As shown in previous works, the absorption rate increases with the concentration of oxidizing agent but decreases with the rise of acidity. This paper presents a thorough kinetic investigation of the liquid-phase reaction of SO₂ for a wide range of H₂O₂ and H₂SO₄ concentrations.Absorption of sulfur dioxide was carried out at 20 °C in a pilot-scale packed column. The experimental data were modelled thanks to the theory of absorption in the fast or moderately fast chemical reaction regimes defined by classical Hatta numbers and depending on the H₂O₂ concentration at a given acidity. For both regimes, a satisfactory agreement was obtained between experimental results and predictions of models including original values of kinetic parameters.     

Pilot plant performance of a SO2 to SO3 oxidation catalyst for flue-gas conditioning

A honeycomb catalyst for the oxidation of endogenous SO₂ from a coal-fired power-station flue-gas has been developed. The catalyst reached a SO₂ to SO₃ conversion of 60 vol.% after 200 h in operation at the pilot plant. When this catalyst is further treated for another 100 h at lab scale to complete its activation, a stable 80 vol.% conversion is obtained. The results have been used to design an industrial unit for flue-gas conditioning to improve the fly ash collection by the electrostatic precipitator in a 220 MW coal-fired power plant.     

碳酸钾-乙醇胺复合溶液吸收烟气中CO2的实验研究

分别以不同浓度的碳酸钾溶液及不同配比的碳酸钾—乙醇胺复合溶液作为吸收剂,以吸收速率和吸收量为指标,研究了吸收剂对烟气中CO2的吸收效果.结果表明,纯碳酸钾溶液吸收效果不佳,而掺入乙醇胺后的吸收效果显著改善,部分复合溶液的吸收效果甚至好于同浓度纯碳酸钾溶液与纯乙醇胺溶液的吸收效果之和,碳酸钾与乙醇胺在吸收过程中存在正交互作用.确定0.6 mol·L-1碳酸钾-0.4mol· L-1乙醇胺复合溶液为最佳的吸收剂,其饱和吸收量最大(0.185 mol)、再生温度最低(105℃)、再生率最高(98.8％).     

CO2 absorption and regeneration of alkali metal-based solid sorbents

Potassium-based sorbents were prepared by impregnation with potassium carbonate on supports such as activated carbon (AC), TiO₂, Al₂O₃, MgO, SiO₂ and various zeolites. The CO₂ capture capacity and regeneration property were measured in the presence of H₂O in a fixed-bed reactor, during multiple cycles at various temperature conditions (CO₂ capture at 60 °C and regeneration at 130–400 °C). Sorbents such as K₂CO₃/AC, K₂CO₃/TiO₂, K₂CO₃/MgO, and K₂CO₃/Al₂O₃, which showed excellent CO₂ capture capacity, could be completely regenerated above 130, 130, 350, and 400 °C, respectively. The decrease in the CO₂ capture capacity of K₂CO₃/Al₂O₃ and K₂CO₃/MgO, after regeneration at temperatures of less than 200 °C, could be explained through the formation of KAl(CO₃)₂(OH)₂, K₂Mg(CO₃)₂, and K₂Mg(CO₃)₂·4(H₂O), which did not completely converted to the original K₂CO₃ phase. In the case of K₂CO₃/AC and K₂CO₃/TiO₂, a KHCO₃ crystal structure was formed during CO₂ absorption, unlike K₂CO₃/Al₂O₃ and K₂CO₃/MgO. This phase could be easily converted into the original phase during regeneration, even at a low temperature (130 °C). Therefore, the formation of the KHCO₃ crystal structure after CO₂ absorption is an important factor for regeneration, even at the low temperature. The nature of support plays an important role for CO₂ absorption and regeneration capacities. In particular, the K₂CO₃/TiO₂ sorbent showed excellent characteristics in CO₂ absorption and regeneration in that it satisfies the requirements of a large amount of CO₂ absorption (mg CO₂/g sorbent) and fast and complete regeneration at a low temperature condition (1 atm, 150 °C).     

单乙醇胺吸收CO2的热力学模型和过程模拟

采用非随机双流体电解质（ENRTL）热力学模型,通过拟合单乙醇胺（MEA）的饱和蒸气压、热容数据,MEA和水（H₂O）二元体系的汽液平衡、热容、混合热数据,以及二氧化碳（CO₂）在MEA水溶液中的溶解度数据,建立了MEA吸收CO₂的热力学模型,并用核磁共振（NMR）组成数据成功地进行了验证。在此模型基础上,利用平衡级模型建立了MEA吸收/解吸CO₂的过程模拟,利用文献中中试工厂数据验证了过程模拟的准确性。对于质量分数为30%的MEA溶液,固定吸收塔CO₂去除率为90%的条件下,当吸收塔液气质量流率比值为2时,再沸器能耗最小,为3.64 GJ·（t CO₂）^-1。     

CO2 capture into aqueous solutions of piperazine activated 2-amino-2-methyl-1-propanol

In this work, experimental data and a simplified vapor–liquid equilibrium (VLE) model for the absorption of CO₂ into aqueous solutions of piperazine (PZ) activated 2-amino-2-methyl-1-propanol (AMP) are reported. The purpose of the work was to find the AMP/PZ system with the highest concentration and cyclic capacity, which could be used in the industry without forming solid precipitations at operational temperatures. The effect of the AMP/PZ ratio and the total concentration level of amine was studied. The highest possible ratio of AMP/PZ, which does not form solid precipitates during the absorption of CO₂ at 40 °C (40 wt% amine), was identified. Considering the maximum loading found in the screening tests for AMP/PZ (3+1.5 M) and for 30 wt% MEA systems, the AMP/PZ system has about 128% higher specific cyclic capacity if operating between 40 and 80 °C, and almost twice the CO₂ partial pressure at 120 °C compared to MEA.     

Energy saving in a CO2 capture plant by MEA scrubbing

The most commonly used process for the CO₂ capture is absorption by means of chemical solvents such as alkanolamines. This consolidated technology can be applied to CO₂ removal from natural gas, refinery gas, and exhaust gas of power plants.This paper focuses on CO₂ capture from exhaust gas by absorption with monoethanolamine (MEA).A commercial simulation software, namely Aspen Plus^®, is used, with Electrolyte-NRTL thermodynamic package where ad hoc parameters, obtained from regression of experimental solubility data for the system CO₂-MEA-H₂O, have been implemented.The comparison among different schemes is based on energy saving. Both the reboiler heat duty and the total equivalent work (which sums up every work and heat contribution in the purification section) are considered as criteria for comparison.     

Ionic liquids for CO2 capture—Development and progress

Innovative off-the-shelf CO₂ capture approaches are burgeoning in the literature, among which, ionic liquids seem to have been omitted in the recent Intergovernmental Panel on Climate Change (IPCC) survey. Ionic liquids (ILs), because of their tunable properties, wide liquid range, reasonable thermal stability, and negligible vapor pressure, are emerging as promising candidates rivaling with conventional amine scrubbing. Due to substantial solubility, room-temperature ionic liquids (RTILs) are quite useful for CO₂ separation from flue gases. Their absorption capacity can be greatly enhanced by functionalization with an amine moiety but with concurrent increase in viscosity making process handling difficult. However this downside can be overcome by making use of supported ionic-liquid membranes (SILMs), especially where high pressures and temperatures are involved. Moreover, due to negligible loss of ionic liquids during recycling, these technologies will also decrease the CO₂ capture cost to a reasonable extent when employed on industrial scale. There is also need to look deeply into the noxious behavior of these unique species. Nevertheless, the flexibility in synthetic structure of ionic liquids may make them opportunistic in CO₂ capture scenarios.     

On the occurence of the mineral trona (Na2CO3.NaHCO3.2H2O) in concrete deterioration products.

Trona has been found amongst the deterioration products of a 30 year old reinforced concrete structure situated on a south-facing headland overlooking the sea. The affected concrete was exposed at the top of a 55m high cliff to the prevailing south west salt-laden winds but was protected by an overhang from direct rainfall. The deterioration appeared to take place due to spalling of successive layers of concrete and resembled the flaking of limestone due to salt crystallisation.     

The absorption of CO2 by amine-potash solutions

CO₂ has been absorbed in a stirred vessel into aqueous solutions of MEA and DEA containing K₂CO₃, K₂SO₄ and Na₂SO₄ at 25° and 11°C. While electrolytes in general appear to increase the rate of reaction between CO₂ and both MEA and DEA, K₂CO₃ increases the rate of reaction of DEA much more than that of MEA. The addition of K₂CO₃ to solutions of DEA increases the absorption rate, in spite of the decrease in the solubility and diffusivity of CO₂. The observations help to explain why DEA is an effective promoter for the absorption and desorption of CO₂ by hot, concentrated potash solutions.     

Investigations into the kinetics and mechanism of gas–solid state processes in MgO–MgR2O4 (R: Al,Cr, Fe) spinels–SO2–O2 system

In refractory ceramics magnesia-spinel materials continue to play an important role for both economic and research reasons. Although their basic properties are considered to be well-known, problems connected with production technology and improvement of application remain to be solved. The aim of this work is to describe and explain the behaviour of spinels in gaseous environment having high concentration of sulfur oxides.     

SO2、CO转化率及SO3、CO2吸收率的计算

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The influence of gas composition on the oxygen electrode reaction in the molten Li2CO3Na2CO3K2CO3 eutectic mixture

Several different electrochemical techniques have been used to study the redox reactions at smooth gold electrodes in molten ternary alkali metal carbonate eutectic mixture equilibrated with different atmopsheric compositions of carbon dioxide and oxygen. The diffusion controlled redox reaction

was identified by chronopotentiometry, which, together with cyclic voltammetry and normal pulse voltammetry, confirmed that both peroxide and oxide ions were present simultaneously. The ratio of peroxide to oxide ions depended on the gas composition. A simple thermodynamic model enabled concentrations of these species to be predicted and correlated with the experimental measurements. The diffusion coefficients of peroxide and oxide ions were deduced from these data.     

Stripper configurations for CO2 capture by aqueous monoethanolamine

Absorption/stripping with amine solvents is a practical tail end technology for CO₂ capture from coal-fired power plants. One of the inhibiting costs of this technology is the energy requirement for solvent regeneration in the stripper, but novel configurations can help reduce this requirement by making the process more reversible. This work looked at several configurations with varying levels of complexity to determine the most useful method for arranging process units. Evaluated configurations included multi-stage flash, multi-pressure columns, and advanced stripping columns. Using a higher number of pressure stages, packing in place of equilibrium flashes, and vapor recompression were all reasonable methods to reduce the overall equivalent work requirement, but the most significant improvement was seen with an interheated column. The interheated column and simple stripper required 33.4 kJ/mol CO₂ and 35.0 kJ/mol CO₂ of work, respectively, at their optimum lean loadings.     

Solubility of Na2SO4, Na2CO3 and their mixture in supercritical water

The solubility of many salts in water decreases dramatically with temperature in the vicinity of the critical point of pure water. Examples of these salts are sulfates of sodium, potassium, lithium and sodium carbonate. These salts are usually produced during supercritical water oxidation (SCWO) and contribute to fouling. The solubility of Na₂CO₃ and Na₂SO₄ has been determined in pure form and in the presence of each other, for the temperature range relevant to SCWO. The experimental procedure was to pass the salt solution through a tube at constant temperature. After a brief initiation period during which no salt sticks to the tube, the salt above the solubility limit deposited on the tube surface. The solution leaving the section was thus at the solubility limit. A rapid decrease in the salt solubility was observed just above the pseudo-critical temperature. For supercritical conditions, the solubility of each salt in the form of a mixture was quite close to the solubility of pure salt. At the highest fluid density considered (480 kg/m³) the presence of Na₂CO₃ reduces the solubility of Na₂SO₄, as might be expected from the “common-ion effect”.