ABSTRACT
Carbon Capture Utilization and Storage technologies are essential mitigation options to reach net-zero CO2 emissions. However, this challenge requires the development of sustainable and economic separation technologies. This work presents a novel CO2 capture technology strategy based on non-dispersive CO2 absorption and membrane vacuum regeneration (MVR) technology, and employs two imidazolium ionic liquids (ILs), [emim][Ac] and [emim][MS], with different behavior to absorb CO2. Continuous absorption-desorption experiments were carried out using polypropylene hollow fiber membrane contactors. The results show the highest desorption behavior in the case of [emim][Ac], with a MVR performance efficiency of 92% at 313 K and vacuum pressure of 0.04 bar. On the other hand, the IL [emim][MS] reached an efficiency of 83% under the same conditions. The MVR technology could increase the overall CO2 capture performance by up to 61% for [emim][Ac] and 21% for [emim][MS], which represents an increase of 26% and 9%, respectively. Moreover, adding 30%vol. demonstrates that the process was only favorable by using the physical IL. The results presented here indicate the interest in membrane vacuum regeneration technology based on chemical ILs, but further techno-economic evaluation is needed to ensure the competitiveness of this novel CO2 desorption approach for large-scale application.
ABSTRACT
Alternative materials are needed to tackle the sustainability of membrane fabrication in light of the circular economy, so that membrane technology keeps playing a role as sustainable technology in CO2 separation processes. In this work, chitosan (CS)-based mixed matrix thin layers have been coated onto commercial polyethersulfone (PES) supports. The CS matrix was loaded by non-toxic 1-Ethyl-3-methylimidazolium acetate ionic liquid (IL) and/or laminar nanoporous AM-4 and UZAR-S3 silicates prepared without costly organic surfactants to improve CO2 permselectivity and mechanical robustness. The CO2/CH4 separation behavior of these membranes was evaluated experimentally at different feed gas composition (CO2/CH4 feed mixture from 20:80 to 70:30%), covering different separation applications associated with this separation. A cross-flow membrane cell model built using Aspen Custom Modeler was used to validate the process performance and relate the membrane properties with the target objectives of CO2 and CH4 recovery and purity in the permeate and retentate streams, respectively. The purely organic IL-CS and mixed matrix AM-4:IL-CS composite membranes showed the most promising results in terms of CO2 and CH4 purity and recovery. This is correlated with their higher hydrophilicity and CO2 adsorption and lower swelling degree, i.e., mechanical robustness, than UZAR-S3 loaded composite membranes. The purity and recovery of the 10 wt.% AM-4:IL-CS/PES composite membrane were close or even surpassed those of the hydrophobic commercial membrane used as reference. This work provides scope for membranes fabricated from renewable or biodegradable polymers and non-toxic fillers that show at least comparable CO2/CH4 separation as existing membranes, as well as the simultaneous feedback on membrane development by the simultaneous correlation of the process requirements with the membrane properties to achieve those process targets.
ABSTRACT
Within the current climate emergency framework and in order to avoid the most severe consequences of global warming, membrane separation processes have become critical for the implementation of carbon capture, storage, and utilization technologies. Mixtures of CO2 and CH4 are relevant energy resources, and the design of innovative membranes specifically designed to improve their separation is a hot topic. This work investigated the potential of modified polydimethylsiloxane and ionic liquid-chitosan composite membranes for separation of CO2 and CH4 mixtures from different sources, such as biogas upgrading, natural gas sweetening, or CO2 enhanced oil recovery. The techno-economic optimization of multistage processes at a real industrial scale was carried out, paying special attention to the identification of the optimal configuration of the hollow fiber modules and the selection of the best membrane scheme. The results demonstrated that a high initial content of CH4 in the feed stream (like in the case of natural gas sweetening) might imply a great challenge for the separation performance, where only membranes with exceptional selectivity might achieve the requirements in a two-stage process. The effective lifetime of the membranes is a key parameter for the successful implementation of innovative membranes in order to avoid severe economic penalties due to excessively frequent membrane replacement. The scale of the process had a great influence on the economic competitiveness of the process, but large-scale installations can operate under competitive conditions with total costs below 0.050 US$ per m3 STP of treated feed gas.
ABSTRACT
Membrane technology is a simple and energy-conservative separation option that is considered to be a green alternative for CO2 capture processes. However, commercially available membranes still face challenges regarding water and chemical resistance. In this study, the effect of water and organic contaminants in the feed stream on the CO2/CH4 separation performance is evaluated as a function of the hydrophilic and permselective features of the top layer of the membrane. The membranes were a commercial hydrophobic membrane with a polydimethylsiloxane (PDMS) top layer (Sulzer Chemtech) and a hydrophilic flat composite membrane with a hydrophilic [emim][ac] ionic liquid-chitosan (IL-CS) thin layer on a commercial polyethersulfone (PES) support developed in our laboratory. Both membranes were immersed in NaOH 1M solutions and washed thoroughly before characterization. The CO2 permeance was similar for both NaOH-treated membranes in the whole range of feed concentration (up to 250 GPU). The presence of water vapor and organic impurities of the feed gas largely affects the gas permeance through the hydrophobic PDMS membrane, while the behavior of the hydrophilic IL-CS/PES membranes is scarcely affected. The effects of the interaction of the contaminants in the membrane selective layer are being further evaluated.
ABSTRACT
In this work, the membrane vacuum regeneration (MVR) process was considered as a promising technology for solvent regeneration in post-combustion CO2 capture and utilization (CCU) since high purity CO2 is needed for a technical valorization approach. First, a desorption test by MVR using polypropylene hollow fiber membrane contactor (PP-HFMC) was carried out in order to evaluate the behavior of physical and physico-chemical absorbents in terms of CO2 solubility and regeneration efficiency. The ionic liquid 1-ethyl-3-methylimidazolium acetate, [emim][Ac], was presented as a suitable alternative to conventional amine-based absorbents. Then, a rigorous two-dimensional mathematical model of the MVR process in a HFMC was developed based on a pseudo-steady-state to understand the influence of the solvent regeneration process in the absorption-desorption process. CO2 absorption-desorption experiments in PP-HFMC at different operating conditions for desorption, varying vacuum pressure and temperature, were used for model validation. Results showed that MVR efficiency increased from 3% at room temperature and 500 mbar to 95% at 310K and 40 mbar vacuum. Moreover, model deviation studies were carried out using sensitivity analysis of Henry's constant and pre-exponential factor of chemical interaction, thus as to contribute to the knowledge in further works.
ABSTRACT
Lignin is one of the three main components of lignocellulosic biomass and must be considered a raw material with attractive applications from an economic and ecological point of view. Therefore, biorefineries must have in mind the most adequate processing to obtain high-quality lignin and the separation tasks that play a key role to improve the purity of the lignin. Separation techniques based on membranes are a promising way to achieve these requirements. In this work, the separation performance of the SILM (Supported Ionic Liquid Membrane) formed with [BMIM][DBP] as IL (Ionic Liquid) and PTFE as membrane support was compared to a nanofiltration (NF) membrane (NP010 by Microdyn-Nadir) and two ultrafiltration (UF) membranes (UF5 and UF10 by Trisep). The SILM showed selective transport of Kraft lignin, lignosulphonate, xylose, and glucose in aqueous solutions. Although it was stable under different conditions and its performance was improved by the integration of agitation, it was not competitive when compared to NF and UF membranes, although the latter ones suffered fouling. The NF membrane was the best alternative for the separation of lignosulphonates from monosaccharides (separation factors around 75 while SILM attained only values lower than 3), while the UF5 membrane should be selected to separate Kraft lignin and monosaccharides (separation factors around 100 while SILM attained only values below 3).
ABSTRACT
A bibliometric analysis based on Scopus database was performed to identify the global research trends related to Supported Ionic Liquid Membranes (SILMs) during the time period from 1995 to 2015. This work tries to improve the understanding of the most relevant research topics and applications. The results from the analysis reveal that only after 2005 the research efforts focused on SILMs became significant, since the references found before that year are scarce. The most important research works on the four main application groups for SILMs defined in this work (carbon dioxide separation, other gas phase separations, pervaporation and liquid phase separations) were summarized in this paper. Carbon dioxide separation appeared as the application that has received by far the most attention according to the research trends during the analysed period. Comments about other significant applications that are gaining attention, such as the employment of SILMs in analytical tasks or their consideration for the production of fuel cells, have been included.
