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AbstractMembrane Technology and Research, Inc. has proposed a hybrid system combining amine scrubbing with membrane technology to reduce energy cost. Previous studies of CO2 absorption mainly focused on coal-fired flue gas with 12% CO2. However, in the hybrid process, the CO2 in the flue gas can be enriched to 20%. Natural gas turbines will have flue gas with as little as 3% CO2。 Based on the arrangement, the hybrid amine/membrane system provides a gas to the system that has double the CO2 concentration of normal flue gas, reduces the volume of gas sent to the capture unit, or reduces the removal requirements for the capture unit.The objective of this work is to minimize the total energy use of stripping concentrated piperazine (PZ) at rich loading when treating flue gas from 3 to 20% inlet CO2. The base-case stripping configuration is the advanced flash stripper with warm rich bypass and cold rich exchanger bypass. . This configuration includes two split cross-exchangers in series, a convective steam heater, a smaller stripper column, a low residence time flash tank, and stripping at high temperature to produce CO2 at 5 to 17bar. Rich loading in 5 and 8m PZ was varied from 0.37 to 0.43mol CO2/mol N. For each rich loading, lean loading was optimized to minimize the total equivalent work. The “Independence” model for PZ in Aspen Plus® was used to simulate the stripping performance.Because 5m PZ has a lower viscosity than 8m PZ, it can achieve a reduced approach temperature in the cross exchanger. The total energy performance for 5m PZ is practically the same as 8m PZ, even though the capacity of 5m PZ is lower. Significantly more energy is required to regenerate solvents with lower rich loading. As CO2 rich loading increases, the equivalent work requirement decreases for the same loading difference between rich and lean.Stripping data for 24 cases, including heat duty, equivalent work, CO2 output pressure, and optimal cold and warm rich bypass were used to build a correlation with CO2 rich and lean loading. The Second Law efficiency based on the ratio of stripping minimum work and total ideal work was introduced to make the most of stripping work. The Second Law efficiency has a maximum value at a specific CO2 loading.

It is crucial to reduce the energy penalties related to CO2 capture processes if CCS is to be implemented at industrial scale. In this context, gas-solid sorption has become a relevant technology. The absence of large amounts of water when using dry solid sorbents and their high heat capacity reduce the energy requirements in the gas-solid sorption CO2 capture process. Depending on the sorbent composition, the gas-solid sorption process carries out at high or low temperatures. High temperature sorbents allow the utilization of waste energy while energy requirements in low temperature processes will be less demanding. This study is focused on the assessment and comparison of the final energy penalty of low-temperature (amine impregnated alumina-based solid particles) and high-temperature solid sorbents capture process (calcium oxide).

Abstract The kinetics of CO 2 absorption in unloaded aqueous ammonia solution were measured using a string of discs contactor with the aqueous ammonia concentrations ranging 0.9–5.4 kmol/m 3 and temperatures ranging 298.3–321.9 K. The reaction rates strongly increase with the concentration and less strongly with temperature. Both the termolecular and zwitterion models were applied in this study as amine solutions. The parameters for both of the models were interpreted. The kinetic rate constants for CO 2 absorption in aqueous ammonia were compared with those for other amines and were found to be around 1/10 that for monoethanolamine. The fitting results for the termolecular mechanism seem more robust than those for the zwitterion mechanism from a statistical perspective.

Abstract The use of water production as a pressure mitigation tool in the context of CO2 storage is widely studied but the impact it might have on the migration behaviour of a buoyant CO2 plume is less well reported. To investigate this further two different scenarios were modelled. In the first, a single water production well was used to draw CO2 along the strike of an open aquifer with a regional dip. Large rates of water production (5–10 times the volume of injected CO2) were required to achieve only small displacements of the CO2 plume. The second scenario investigated to what extent an induced hydraulic gradient might spill CO2 already stored in a structural trap. Here the effects were more pronounced with over 90% of the CO2 being spilled at a water cycling rate of 10 Mt per year (corresponding to a hydraulic gradient of 1.28 bar/km). The modelling was tested by the real case at Sleipner where CO2 migration in the Utsira Sand is potentially impacted by water production at the nearby Volve field. Simulations concluded that the CO2 plume at Sleipner should not be materially affected by water production from Volve and this is supported by the time-lapse seismics.

Biodiesel can be produced from vegetable oils, animal fats, and waste cooking oils by transesterification with ethanol (also called ethanolysis) in order to substitute fossil fuels. In this work, the batch ethanolysis of high oleic sunflower oil was transferred into a continuous microstructured device, which induces a better control of heat and mass transfers. Various parameters were studied, notably the initial ethanol to oil molar ratio. An innovative method using NIR spectroscopy was also developed to on-line monitor the transesterification reaction of high oleic sunflower oil with ethanol in microreactors (circular PFA tube 1/1600 OD, 0.0200 ID). The reactions were monitored directly in the microreactors through sequential scans of the reaction medium by the means of an adequate probe. The asset of the method is that no sample collection or preparation is necessary. Partial Least Squares regression was used to develop calibration and prediction models between NIR spectral data and analytical data obtained by a reference method (gas chromatography with flame ionization detection, GC–FID). This method is fast, safe, reliable, nondestructive and inexpensive contrary to conventional procedures, such as gas chromatography and high performance liquid chromatography generally used to determine the composition of crude transesterification medium.

AbstractThe present studies report the use of an ecofriendly biomass Ficus religiosa in untreated (UFR) and xanthate treated (XFR) forms for the Cd (II) ions removal in a fixed bed column. FTIR, SEM‐EDS, BET surface area, and elemental analysis (CHNS) techniques were used to characterize the biosorbents. The acquired data supported FTIR findings regarding the nature of functional groups present in the materials. Packed bed continuous flow studies explored the effects of various parameters such as Cd (II) ion concentration (100 mg/L–300 mg/L), bed heights (5 cm–30 cm), pH (3–5), at a constant linear flow rate (~1.13 cm/min). The obtained S‐shaped breakthrough curves indicated the efficiency of the packed bed for the Cd (II) removal. Breakthrough time and exhaust times increased (67.5 min–390 min and 292.5 min–1852.5 min) (97.5 min–442.5 min and 345 min–1920 min) for unmodified and modified respectively with bed heights. The BDST, Thomas, and Yoon‐Nelson models were used to evaluate the experimental results. The Yoon‐Nelson model describes the breakthrough data more efficiently compared to other models. Under similar conditions, the modified material exhibited 400% increased capacity (55.20 mg/g) than that of unmodified material (13.33 mg/g). Thus, xanthate modification significantly enhanced the capacity for Cd (II) ions from aqueous solutions.Practitioner Points Xanthate modification of Ficus religiosa is an environmentally friendly process. Modified and unmodified materials were utilized for Cd (II) removal in fixed bed column process which is industrially viable process. Low inlet Cd (II) concentration at pH 5 and higher bed height favored the continuous flow process at fixed flow rate. Modification caused an increase of about 400% in the capacity of material.

Abstract This study demonstrates the coupling of Ionic liquids (ILs) with a membrane contactor for post-combustion CO2 capture at moderate pressures and temperatures. ILs 1-ethyl-3-methylimidazolium methyl sulfate([emim][MeSO4]), 1-ethyl-3-methylimidazolium dicyanamide([emim][DCA]), 1-ethyl-3-methylimidazolium ethyl sulfate([emim][EtSO4]) and 1-ethyl-3-methylimidazolium acetate ([emim][Ac]) were selected due to their high thermal stability, moderate viscosity and surface tension, as well as high CO2 solubility. No wetting conditions were confirmed for the polypropylene membrane by measuring contact angle, liquid entry pressure (LEP) and SEM of fiber surface before and after the operation. ILs were recirculated in the setup until reaching pseudo-steady-state. All four ILs were able to capture a substantial amount of CO2 during the specified operation time. Initially, very high values of CO2 mass transfer flux and experimental overall mass transfer coefficient were obtained which further decreased with operation time and reached a nearly constant value at pseudo-steady-state. Effect of CO2 loading of the ILs and temperature on enhancement factor and first order rate constant were evaluated. The absorption behavior and kinetics were strongly influenced by the CO2 concentration in the ILs, which divides the absorption process in two steps; an initial faster absorption at the gas-liquid interface and later slower absorption in the bulk of the IL. Finally, a pseudo-steady-state modelling approach was implemented and validated.