Enhancing Absorption Performance of CO2 by Amine Solution through the Spiral Wired Channel in Concentric Circular Membrane Contactors

The CO2 absorption rate by using a Monoethanolamide (MEA) solution through the spiral wired channel in concentric circular membrane contactors under both concurrent-flow and countercurrent-flow operations was investigated experimentally and theoretically. The one-dimensional mathematical modeling equation developed for predicting the absorption rate and concentration distributions was solved numerically using the fourth Runge–Kutta method under various absorbent flow rate, CO2 feed flow rate and inlet CO2 concentration in the gas feed. An economical viewpoint of the spiral wired module was examined by assessing both absorption flux improvement and power consumption increment. Meanwhile, the correlated average Sherwood number to predict the mass-transfer coefficient of the CO2 absorption mechanisms in a concentric circular membrane contactor with the spiral wired annulus channel is also obtained in a generalized and simplified expression. The theoretical predictions of absorption flux improvement were validated by experimental results in good agreements. The amine solution flowing through the annulus of a concentric circular tube, which was inserted in a tight-fitting spiral wire in a small annular spacing, could enhance the CO2 absorption flux improvement due to reduction of the concentration polarization effect. A larger concentration polarization coefficient (CPC) was achieved in the countercurrent-flow operations than that in concurrent-flow operations for various operations conditions and spiral-wire pitches. The absorption flux improvement for inserting spiral wire in the concentric circular module could provide the maximum relative increment up to 46.45%.

The Kinetics Investigation of CO2 Absorption into TEA and DEEA Amine Solutions Containing Carbonic Anhydrase

Tertiary amines have been used as alternative absorbents for traditional primary and secondary amines in the process of carbon capture. However, the carbon dioxide (CO2) absorption rates in these kinds of amine are relatively slow, which implies greater investment and construction costs and limits the large-scale application of carbon capture. Carbonic anhydrase (CA) is considered to be an ideal homogeneous catalyst for accelerating the rate of CO2 into aqueous amine solution. In this work, CO2 absorption combining CA with two single aqueous tertiary amines, namely triethanolamine (TEA) and 2-(diethylamino)ethanol (DEEA), was studied by use of the stopped-flow apparatus over temperature ranging from 293 to 313 K. The concentrations of selected aqueous amine solution and CA used in the experiment were ranging among 0.1–0.5 kmol/m3 and 0–50 g/m3 , respectively. Compared to the solution without the addition of CA, the pseudo first-order reaction rate in the presence of CA (k0,withCA) is significantly increased. The values of k0,withCA have been calculated by a new kinetics model. The results of experimental and calculated k0,amine and k0,withCA in CO2-amine-H2O solutions were also investigated,respectively.

Selective Electrochemical Regeneration of Aqueous Amine Solutions to Capture CO2 and to Convert H2S into Hydrogen and Solid Sulfur

Removing CO2 from natural gas or biogas in the presence of H2S is technically challenging and expensive as it often requires separation of both acid gases from the gas, typically using an aqueous amine solution, followed by separation of CO2 from H2S and conversion of H2S into solid S. In this work, the proof of concept of electrochemical, instead of thermal, regeneration of an aqueous amine solution is developed. This invention might be a very promising technology and has several advantages. It has H2S versus CO2 selectivity of 100%, can directly convert H2S into S and H2, and is economically competitive with CO2 desorption energy around 100 kJmol−1 and H2S conversion around 200 kJmol−1. If renewable energy is used for electrochemical regeneration, CO2 emissions due to the CO2 capture process can be significantly reduced.

Modelling and Simulation of Acid Gas Absorption from Natural Gas by Amine Solution Using Aspen HYSYS

This work has been carried out to model and simulate a typical acid gas absorption process using Aspen HYSYS process simulator. The chemical components involved in the process development were water, methane, ethane, propane, higher alkanes, carbon dioxide, hydrogen sulphide, nitrogen and amines: monoethanolamine (MEA), diethanolamine (DEA), triethanolamine (TEA) and methyldiethanolamine (MDEA). The fluid package selected for the simulation before entering the simulation environment was Acid Gas – Chemical Solvents. In the simulation environment, the model was developed by picking an absorber from the Model Palette, placing it and assigning the input and the output streams involved before inputting the parameters required for model convergence. The carbon dioxide-rich feed gas was made to enter the absorber at the bottom inlet stream while the lean amine stream entered at the top inlet and showered down on the uprising gas thereby trapping the carbon dioxide molecules within the gas. The top product from the absorber was the treated gas while the amine solution and the trapped carbon dioxide left the absorber as the bottom product. Different simulations were run to investigate the performance of the amines under the same operating conditions. It was discovered that, of all the four amine solvents considered in this work for the removal of carbon dioxide by chemical absorption, MEA had the highest efficiency but would require more dehydration because it had the highest water content. DEA was also found to scrub the carbon dioxide down to acceptable levels. However, TEA and MDEA barely scrubbed any carbon dioxide under these conditions, as their carbon dioxide compositions were found to be unacceptable. The analyses of the results obtained from the simulations indicated that Aspen HYSYS can be used to study the process of acid gas absorption successfully.

Modeling of Nanofiltration Process Using DSPM-DE Model for Purification of Amine Solution

The formation of heat stable salts (HSS) during the natural gas sweetening process by amine solvent causes many problems such as corrosion, foaming, capacity reduction, and amine loss. A modeling study was carried out for the removal of HSS ions from amine solution using nanofiltration (NF) membrane process that ensures the reuse of amine solution for gas sweetening. This model studies the physics of the nanofiltration process by adjusting and investigating pore radius, the effects of membrane charge, and other membrane characteristics. In this paper, the performance of the ternary ions was investigated during the removal process from methyl di-ethanol amine solution by the nanofiltration membrane process. Correlation between feed concentration and permeate concentration, using experimental results with mathematical correlation as Ci,p = f (Ci,f) was used in modeling. The results showed that the calculated data from the model provided a good agreement with experimental results (R2 = 0.90–0.75). Also, the effect of operating conditions (including feed pressure and feed flow rate on ions rejection and recovery ratio across the flat-sheet membrane) was studied. The results showed that the recovery and rejection ratios of the NF membrane depend on the driving pressure across the membrane. While the driving pressure is affected by the feed flow conditions and feed pressure.