Browse
Submit Data
Databases
API
Help

Dataset Information

22 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Hybrid Ionic Liquid Capsules for Rapid CO₂ Capture.

ABSTRACT: The CO₂ absorption by ionic liquids (ILs) were enhanced by the use of hybrid capsules composed of a core of IL and shell of polyurea and alkylated graphene oxide (GO). These composite structures were synthesized using a Pickering emulsion as a template and capsules of two different ILs were prepared. The contribution of the encapsulated IL on the CO₂ absorption of the capsules is consistent with agitated neat IL, but with improved kinetics of absorption across different pressures. This novel materials design allows for CO₂ to be absorbed significantly faster compared to bulk IL and provides insight into improved carbon capture technologies.

SUBMITTER: Huang Q

PROVIDER: S-EPMC7837423 | biostudies-literature | 2019 Jun

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Publications

Hybrid Ionic Liquid Capsules for Rapid CO2 Capture.

Huang Qianwen Q Luo Qinmo Q Wang Yifei Y Pentzer Emily E Gurkan Burcu B

Industrial & engineering chemistry research 20190524 24

The CO2 absorption by ionic liquids (ILs) were enhanced by the use of hybrid capsules composed of a core of IL and shell of polyurea and alkylated graphene oxide (GO). These composite structures were synthesized using a Pickering emulsion as a template and capsules of two different ILs were prepared. The contribution of the encapsulated IL on the CO2 absorption of the capsules is consistent with agitated neat IL, but with improved kinetics of absorption across different pre ...[more]

PMID: 33505108

Similar Datasets

Liquid marble-derived solid-liquid hybrid superparticles for CO2 capture.

Project description:The design of effective CO2 capture materials is an ongoing challenge. Here we report a concept to overcome current limitations associated with both liquid and solid CO2 capture materials by exploiting a solid-liquid hybrid superparticle (SLHSP). The fabrication of SLHSP involves assembly of hydrophobic silica nanoparticles on the liquid marble surface, and co-assembly of hydrophilic silica nanoparticles and tetraethylenepentamine within the interior of the liquid marble. The strong interfacial adsorption force and the strong interactions between amine and silica are identified to be key elements for high robustness. The developed SLHSPs exhibit excellent CO2 sorption capacity, high sorption rate, long-term stability and reduced amine loss in industrially preferred fixed bed setups. The outstanding performances are attributed to the unique structure which hierarchically organizes the liquid and solid at microscales.

| S-EPMC6478824 | biostudies-literature

Integrated CO2 capture-fixation chemistry via interfacial ionic liquid catalyst in laminar gas/liquid flow.

Project description:Simultaneous capture of carbon dioxide (CO2) and its utilization with subsequent work-up would significantly enhance the competitiveness of CO2-based sustainable chemistry over petroleum-based chemistry. Here we report an interfacial catalytic reaction platform for an integrated autonomous process of simultaneously capturing/fixing CO2 in gas-liquid laminar flow with subsequently providing a work-up step. The continuous-flow microreactor has built-in silicon nanowires (SiNWs) with immobilized ionic liquid catalysts on tips of cone-shaped nanowire bundles. Because of the superamphiphobic SiNWs, a stable gas-liquid interface maintains between liquid flow of organoamines in upper part and gas flow of CO2 in bottom part of channel. The intimate and direct contact of the binary reagents leads to enhanced mass transfer and facilitating reactions. The autonomous integrated platform produces and isolates 2-oxazolidinones and quinazolines-2,4(1H,3H)-diones with 81-97% yields under mild conditions. The platform would enable direct CO2 utilization to produce high-valued specialty chemicals from flue gases without pre-separation and work-up steps.

| S-EPMC5343516 | biostudies-literature

Preparation of Polyimide/Ionic Liquid Hybrid Membrane for CO2/CH4 Separation.

Project description:Imidazole ionic liquids (ILs) have good affinity and good solubility for carbon dioxide (CO2). Such ionic liquids, combined with polyimide membrane materials, can solve the problem that, today, CO2 is difficult to separate and recover. In this study, the ionic liquid (IL) of 1-ethyl-3-methylimidazolium tetrafluoroborate (IL1), 1-pentyl-3-methylimidazolium tetrafluoroborate (IL2), 1-octyl-3-methylimidazolium tetrafluoroborate (IL3), and 1-dodecylimidazolium tetrafluoroborate (IL4) with different contents were added to a polyimide matrix, and a series of polyimide membranes blended with ionic liquid were prepared using a high-speed mixer. The mechanical properties and gas separation permeability of the membranes were investigated. Among them, the selectivity of the PI/IL3 membrane for CO2/CH4 was 180.55, which was 2.5 times higher than the PI membrane, and its CO2 permeability was 16.25 Barrer, which exceeded the Robeson curve in 2008; the separation performance of the membrane was the best in this work.

| S-EPMC10856979 | biostudies-literature

Improving CO2 photoconversion with ionic liquid and Co single atoms.

Project description:Photocatalytic CO2 conversion promises an ideal route to store solar energy into chemical bonds. However, sluggish electron kinetics and unfavorable product selectivity remain unresolved challenges. Here, an ionic liquid, 1-ethyl-3-methylimidazolium tetrafluoroborate, and borate-anchored Co single atoms were separately loaded on ultrathin g-C3N4 nanosheets. The optimized nanocomposite photocatalyst produces CO and CH4 from CO2 and water under UV-vis light irradiation, exhibiting a 42-fold photoactivity enhancement compared with g-C3N4 and nearly 100% selectivity towards CO2 reduction. Experimental and theoretical results reveal that the ionic liquid extracts electrons and facilitates CO2 reduction, whereas Co single atoms trap holes and catalyze water oxidation. More importantly, the maximum electron transfer efficiency for CO2 photoreduction, as measured with in-situ μs-transient absorption spectroscopy, is found to be 35.3%, owing to the combined effect of the ionic liquid and Co single atoms. This work offers a feasible strategy for efficiently converting CO2 to valuable chemicals.

| S-EPMC10020152 | biostudies-literature

Functionalized Ionic Liquids for CO2 Capture under Ambient Pressure.

Project description:Ionic liquids (ILs) have been widely explored as alternative solvents for carbon dioxide (CO2) capture and utilization. However, most of these processes are under pressures significantly higher than atmospheric level, which not only levies additional equipment and operation costs, but also makes the large-scale CO2 capture and conversion less practical. In this study, we rationally designed glycol ether-functionalized imidazolium, phosphonium and ammonium ILs containing acetate (OAc-) or Tf2N- anions, and found these task-specific ILs could solubilize up to 0.55 mol CO2 per mole of IL (or 5.9 wt% CO2) at room temperature and atmospheric pressure. Although acetate anions enabled a better capture of CO2, Tf2N- anions are more compatible with alcohol dehydrogenase (ADH), which is a key enzyme involved in the cascade enzymatic conversion of CO2 to methanol. Our promising results indicate the possibility of CO2 capture under ambient pressure and its enzymatic conversion to valuable commodity.

| S-EPMC10254919 | biostudies-literature

Alkylimidazolium-based ionic liquids with tailored anions and cations for CO2 capture.

Project description:A systematic investigation was conducted in the present study to determine how various cations and anions affected the solubility of CO2. To investigate the influence of different cations and anions on the solubility of CO2, twelve ILs were synthesized, characterized, and utilized. These ILs comprised five distinct anions (dioctylsulfosuccinate [DOSS], triflouromethanesulfonate [TFMS], dodecylsulfate [DDS], 3-sulfobezoate [SBA], and benzene sulfonate [BS]), and four distinct cations (1-butyl-3-propanenitrile imidazolium [C2CN Bim], 1-hexyl-3-propanenitrile imidazolium [C2CN Him], 1-octyl-3-propanenitrile imidazolium [C2CN Oim], and 1-decyl-3-propanenitrile imidazolium [C2CN Dim]). The synthesized ILs were characterized using NMR and elemental analysis. Their moisture and halide contents were determined. The gravimetric method (MSB) was employed to determine the solubility of CO2 at various pressures (20, 15, 10, 5, and 1 bar). In addition, the effects of temperature on the solubility of CO2 were investigated. The constant of Henry's law (kH) was also calculated, along with thermodynamic properties including standard enthalpy (H0), entropy (S0), and Gibbs free energy (G0).

| S-EPMC10823357 | biostudies-literature

Combined Superbase Ionic Liquid Approach to Separate CO2 from Flue Gas.

Project description:Superbase ionic liquids (ILs) with a trihexyltetradecylphosphonium cation and a benzimidazolide ([P66614][Benzim]) or tetrazolide ([P66614][Tetz]) anion were investigated in a dual-IL system allowing the selective capture and separation of CO2 and SO2, respectively, under realistic gas concentrations. The results show that [P66614][Tetz] is capable of efficiently capturing SO2 in preference to CO2 and thus, in a stepwise separation process, protects [P66614][Benzim] from the negative effects of the highly acidic contaminant. This results in [P66614][Benzim] maintaining >53% of its original CO2 uptake capacity after 30 absorption/desorption cycles in comparison to the 89% decrease observed after 11 cycles when [P66614][Tetz] was not present. Characterization of the ILs post exposure revealed that small amounts of SO2 were irreversibly absorbed to the [Benzim]- anion responsible for the decrease in CO2 capacity. While optimization of this dual-IL system is required, this feasibility study demonstrates that [P66614][Tetz] is a suitable sorbent for reversibly capturing SO2 and significantly extending the lifetime of [P66614][Benzim] for CO2 uptake.

| S-EPMC9326967 | biostudies-literature

CO₂ Capture and Separation Properties in the Ionic Liquid 1-n-Butyl-3-Methylimidazolium Nonafluorobutylsulfonate.

Project description:Recently, the use of ionic liquids (ILs) for carbon capture and separation processes has gained great interest by many researchers due to the high solubility of CO₂ in ILs. In the present work, solubility measurements of CO₂ in the novel IL 1-n-butyl-3-methylimidazolium nonafluorobutylsulfonate [C₄mim][CF₃CF₂CF₂CF₂SO₃] were performed with a high-pressure view-cell technique in the temperature range from 293.15 to 343.15 K and pressures up to about 4.2 MPa. For comparison, solubilities of H₂, N₂, and O₂ in the IL were also measured at 323.15 K via the same procedure. The Krichevsky-Kasarnovsky equation was employed to correlate the measured solubility data. Henry's law constants, enthalpies, and entropies of absorption for CO₂ in the IL were also determined and presented. The CO₂ solubility in this IL was compared with other ILs sharing the same cation. It was shown that the solubility of CO₂ in these ILs follows the sequence: [C₄mim][CF₃CF₂CF₂CF₂SO₃] ≈ [C₄mim][Tf₂N] > [C₄mim][CF₃CF₂CF₂COO] > [C₄mim][BF₄], and the solubility selectivity of CO₂ relative to O₂, N₂, and H₂ in [C₄mim][CF₃CF₂CF₂CF₂SO₃] was 8, 16, and 22, respectively. Furthermore, this IL is regenerable and exhibits good stability. Therefore, the IL reported here would be a promising sorbent for CO₂.

| S-EPMC5453234 | biostudies-other

Supported Imidazolium-Based Ionic Liquids on a Polysulfone Matrix for Enhanced CO2 Capture.

Project description:The present work demonstrates the potential for improved CO2 capture capabilities of ionic liquids (ILs) by supporting them on a polysulfone polymeric matrix. CO2 is one of the main gases responsible for the greenhouse effect and is a focus of The European Commission, which committed to diminishing its emission to 55% by 2023. Various ILs based on combinations of 1-butyl-3-methyl- imidazolium cations and different anions (BMI·X) were synthesized and supported on a polysulfone porous membrane. The influence of the membrane structure and the nature of ILs on the CO2 capture abilities were investigated. It was found that the membrane's internal morphology and its surface characteristics influence its ILs sorption capacity and CO2 solubility. In most of the studied configurations, supporting ILs on porous structures increased their contact surface and gas adsorption compared to the bulk ILs. The phenomenon was strongly pronounced in the case of ILs of high viscosity, where supporting them on porous structures resulted in a CO2 solubility value increase of 10×. Finally, the highest CO2 solubility value (0.24 molCO2/molIL) was obtained with membranes bearing supported ILs containing dicarboxylate anion (BMI.MAL).

| S-EPMC9698076 | biostudies-literature

Reviewing and screening ionic liquids and deep eutectic solvents for effective CO2 capture.

Project description:CO2 capture is essential for both mitigating CO2 emissions and purifying/conditioning gases for fuel and chemical production. To further improve the process performance with low environmental impacts, different strategies have been proposed, where developing liquid green absorbent for capturing CO2 is one of the effective options. Ionic liquids (IL)/deep eutectic solvents (DES) have recently emerged as green absorbents with unique properties, especially DESs also benefit from facile synthesis, low toxicity, and high biodegradability. To promote their development, this work summarized the recent research progress on ILs/DESs developed for CO2 capture from the aspects of those physical- and chemical-based, and COSMO-RS was combined to predict the properties that are unavailable from published articles in order to evaluate their performance based on the key properties for different IL/DES-based technologies. Finally, top 10 ILs/DESs were listed based on the corresponding criteria. The shared information will provide insight into screening and further developing IL/DES-based technologies for CO2 capture.

| S-EPMC9399623 | biostudies-literature