A systematic approach to design task-specific ionic liquids and their optimal operating conditions

2016 ◽  
Vol 1 (1) ◽  
pp. 109-121 ◽  
Author(s):  
Fah Keen Chong ◽  
Dominic C. Y. Foo ◽  
Fadwa T. Eljack ◽  
Mert Atilhan ◽  
Nishanth G. Chemmangattuvalappil
Keyword(s):  
Ionic Liquid ◽  
Ionic Liquids ◽  
Design Problem ◽  
Systematic Approach ◽  
Operating Conditions ◽  
Optimal Operating ◽  
Design Task

The contribution of this work is the introduction to identification of optimal operating conditions when simultaneously solving an ionic liquid design problem.

Ionic Liquid Based CO2 Capturing Fuel Cell for Greenhouse Gas Reduction

2008 ◽  
Vol 1082 ◽  
Author(s):  
Michal V. Wolkin ◽  
Raphael Stumpp ◽  
Karl Littau
Keyword(s):  
Ionic Liquid ◽  
Ionic Liquids ◽  
Fuel Cell ◽  
Cost Effective ◽  
Operating Conditions ◽  
Capture Process ◽  
Aerospace Applications ◽  
Effective Removal ◽  
Co2 Capturing ◽  
Cell Electrolytes

ABSTRACTRoom-temperature ionic liquids are utilized in a new CO2 capturing fuel cell. The cell is aimed at the efficient and cost effective removal of CO2 emitted from transportation related sources. The CO2 is captured from the atmosphere and is later converted into carbon free synthetic fuel such as methanol. In this study we optimized the operating conditions and the cell electrolytes. With ionic liquids such as 1-Butyl-1-methylpyrrolidinium dicyanamide, the extraction efficiencies increased to ∼20% while simultaneously making the capture process more robust. The ionic liquid approach is also compared to existing aqueous electrochemical CO2 concentration previously proposed by NASA for aerospace applications but with much lower efficiencies.

scholarly journals Elucidating the Doping Mechanism in Fluorene-Dithiophene Based Hole Selective Layer Employing Ultra-Hydrophobic Ionic Liquid Dopant

2020 ◽  
Author(s):  
Navind Harindu Hemasiri ◽  
Samrana Kazim ◽  
Laura Calio ◽  
Sanghyun Paek ◽  
Manuel Salado ◽  
...  
Keyword(s):  
Ionic Liquid ◽  
Ionic Liquids ◽  
Solar Cells ◽  
Film Formation ◽  
Perovskite Solar Cells ◽  
Hole Mobility ◽  
Hole Transport ◽  
Operating Conditions ◽  
Hydrophobic Ionic Liquid ◽  
Additive Materials

<p>Perovskite solar cells have set a new milestone in terms of efficiencies in the thin film photovoltaics category. Long-term stability of perovskite solar cells is of paramount importance but remains a challenging task. The lack of perovskite solar cells stability in real-time operating conditions erodes and impedes commercialization. Further improvements are essential with a view to delivering longer-lasting photovoltaic (PV) performances. An ideal path in this direction will be to identify novel dopants for boosting the conductivity and hole mobility of hole transport materials (HTMs), and by so doing the usage of hygroscopic and deliquescent additive materials can be avoided. Pyridine-based ionic liquids represent a well-known class of ultra-hydrophobic materials, which are suitable for their application in opto-electrical devices. The present work demonstrates the employment of ionic liquids into a dissymmetric fluorene-dithiophene, FDT (2’,7’ -bis(bis(4-methoxyphenyl)amino) spiro[cyclopenta[2,1-b:3,4-b’]dithiophene-4,9’-fluorene]) based HTM to understand the doping mechanisms. <i>N</i>-heterocyclic hydrophobic ionic liquid, 1-butyl-3-methylpyidinium bis(trifluoromethylsulfonyl)imide (BMP<i>y</i>TFSI) as p-type dopant for FDT was found to increase the conductivity of FDT, to higher geometrical capacitance, to facilitate homogeneous film formation, and to enhance device stability. Our findings open up a broad range of hole-transport materials to control the degradation of the underlying water-sensitive active layer by substituting hygroscopic element. </p>

scholarly journals Ionic liquid-modified MCM-41-polymer mixed matrix membrane for butanol pervaporation

2019 ◽  
Vol 6 (7) ◽  
pp. 190291 ◽  
Author(s):  
Yifang Li ◽  
Dandan Yan ◽  
Yanhui Wu
Keyword(s):  
Ionic Liquid ◽  
Ionic Liquids ◽  
Separation Factor ◽  
Mesoporous Molecular Sieve ◽  
Operating Conditions ◽  
Mixed Matrix Membranes ◽  
Mixed Matrix Membrane ◽  
Permeation Flux ◽  
Mixed Matrix ◽  
Mcm 41

Because of the preferential butanol selectivity of some ionic liquids (ILs), an increasing amount of research has appeared regarding their application in butanol separation. In this research, two ionic liquids, namely, 1-ethyl-3-vinylimidazolium bis[(trifluoromethyl)sulfonyl]imide ([EVIM][Tf 2 N], IL1) and N -octyl-pyridinium bis[(trifluoromethyl)sulfonyl]imide ([OMPY][Tf 2 N], IL2), were applied to modify a mesoporous molecular sieve MCM-41. The IL-modified MCM-41 samples were characterized by XPS, BET, XRD, SEM and TEM. The ionic liquid-modified MCM-41 was incorporated into the polymer PEBA to prepare mixed matrix membranes to study the influences of the filling of IL-modified MCM-41 and operating conditions on the performance of the mixed matrix membrane for butanol pervaporation. The results indicated that the pervaporation performance of the PEBA membrane was enhanced by the incorporation of IL-modified MCM-41. When the temperature of the feeding liquid was 35°C and the mass fraction of butanol was 2.5 wt%, the 5% MCM-41-IL2-PEBA membrane showed a permeation flux of 421.7 g m −2 h −1 and a separation factor of 25.4. The permeation flux and the separation factor of the membrane increased as the temperature of the feeding liquid increased. The results of the long-period experiment suggested that the 5% MCM-41-IL2-PEBA membrane exhibited high stability within 100 h of operation.

scholarly journals Elucidating the Doping Mechanism in Fluorene-Dithiophene Based Hole Selective Layer Employing Ultra-Hydrophobic Ionic Liquid Dopant

2020 ◽  
Author(s):  
Navind Harindu Hemasiri ◽  
Samrana Kazim ◽  
Laura Calio ◽  
Sanghyun Paek ◽  
Manuel Salado ◽  
...  
Keyword(s):  
Ionic Liquid ◽  
Ionic Liquids ◽  
Solar Cells ◽  
Film Formation ◽  
Perovskite Solar Cells ◽  
Hole Mobility ◽  
Hole Transport ◽  
Operating Conditions ◽  
Hydrophobic Ionic Liquid ◽  
Additive Materials

<p>Perovskite solar cells have set a new milestone in terms of efficiencies in the thin film photovoltaics category. Long-term stability of perovskite solar cells is of paramount importance but remains a challenging task. The lack of perovskite solar cells stability in real-time operating conditions erodes and impedes commercialization. Further improvements are essential with a view to delivering longer-lasting photovoltaic (PV) performances. An ideal path in this direction will be to identify novel dopants for boosting the conductivity and hole mobility of hole transport materials (HTMs), and by so doing the usage of hygroscopic and deliquescent additive materials can be avoided. Pyridine-based ionic liquids represent a well-known class of ultra-hydrophobic materials, which are suitable for their application in opto-electrical devices. The present work demonstrates the employment of ionic liquids into a dissymmetric fluorene-dithiophene, FDT (2’,7’ -bis(bis(4-methoxyphenyl)amino) spiro[cyclopenta[2,1-b:3,4-b’]dithiophene-4,9’-fluorene]) based HTM to understand the doping mechanisms. <i>N</i>-heterocyclic hydrophobic ionic liquid, 1-butyl-3-methylpyidinium bis(trifluoromethylsulfonyl)imide (BMP<i>y</i>TFSI) as p-type dopant for FDT was found to increase the conductivity of FDT, to higher geometrical capacitance, to facilitate homogeneous film formation, and to enhance device stability. Our findings open up a broad range of hole-transport materials to control the degradation of the underlying water-sensitive active layer by substituting hygroscopic element. </p>

Mapping the “Extra Solvent Power, ESP” of Ionic Liquids for Monomers, Polymers and Globular Nanoparticles

2017 ◽  
Author(s):  
Jose A. Pomposo
Keyword(s):  
Ionic Liquid ◽  
Ionic Liquids ◽  
Linear Polymers ◽  
Green Solvents ◽  
Ionic Polymers ◽  
First Time ◽  
Solvent Power

Understanding the miscibility behavior of ionic liquid (IL) / monomer, IL / polymer and IL / nanoparticle mixtures is critical for the use of ILs as green solvents in polymerization processes, and to rationalize recent observations concerning the superior solubility of some proteins in ILs when compared to standard solvents. In this work, the most relevant results obtained in terms of a three-component Flory-Huggins theory concerning the “Extra Solvent Power, ESP” of ILs when compared to traditional non-ionic solvents for monomeric solutes (case I), linear polymers (case II) and globular nanoparticles (case III) are presented. Moreover, useful ESP maps are drawn for the first time for IL mixtures corresponding to case I, II and III. Finally, a potential pathway to improve the miscibility of non-ionic polymers in ILs is also proposed.

Dynamics of Ion Locking in Doubly Polymerized Ionic Liquids

2020 ◽  
Author(s):  
Swati Arora ◽  
Julisa Rozon ◽  
Jennifer Laaser
Keyword(s):  
Dielectric Constant ◽  
Ionic Liquid ◽  
Ionic Liquids ◽  
Ion Pairs ◽  
Polymer Chains ◽  
Ion Motion ◽  
Charged Species ◽  
Broadband Dielectric Spectroscopy ◽  
Covalently Linked ◽  
Insight Into

<div>In this work, we investigate the dynamics of ion motion in “doubly-polymerized” ionic liquids (DPILs) in which both charged species of an ionic liquid are covalently linked to the same polymer chains. Broadband dielectric spectroscopy is used to characterize these materials over a broad frequency and temperature range, and their behavior is compared to that of conventional “singly-polymerized” ionic liquids (SPILs) in which only one of the charged species is attached to the polymer chains. Polymerization of the DPIL decreases the bulk ionic conductivity by four orders of magnitude relative to both SPILs. The timescales for local ionic rearrangement are similarly found to be approximately four orders of magnitude slower in the DPILs than in the SPILs, and the DPILs also have a lower static dielectric constant. These results suggest that copolymerization of the ionic monomers affects ion motion on both the bulk and the local scales, with ion pairs serving to form strong physical crosslinks between the polymer chains. This study provides quantitative insight into the energetics and timescales of ion motion that drive the phenomenon of “ion locking” currently under investigation for new classes of organic electronics.</div>

Studies of microbial acclimation to hard chemicals on the basis of respiratory quinone profiles and kinetic analyses

1996 ◽  
Vol 34 (5-6) ◽  
pp. 249-256 ◽  
Author(s):  
Hong-Ying Hu ◽  
Mamie Nozawa ◽  
Koichi Fujie ◽  
Tsuyoshi Makabe ◽  
Kohei Urano
Keyword(s):  
Pseudomonas Aeruginosa ◽  
Population Dynamics ◽  
Volatile Substance ◽  
Operating Conditions ◽  
Biological Wastewater Treatment ◽  
Basic Information ◽  
Optimal Operating ◽  
Respiratory Quinone ◽  
Treatment Processes ◽  
Quinone Profile

The population dynamics of microbes in the biological wastewater treatment processes such as a submerged biofilter was investigated to obtain basic information to determine the optimal operating conditions. The effects of coexistence of biodegradable substances such as glucose and peptone on the acclimation of microbes in the biofilm to hard chemicals such as acrylonitrile (AN), which is poorly biodegradable and a volatile substance, was investigated on the basis of the respiratory quinone profile. Kinetic study of the removal of AN in the course of acclimation of microbes was investigated using a laboratory-scale submerged biofilter as well. It was ascertained that the acclimation of the microbes to AN was accelerated by coexistence of biodegradable substances, and the microbial phase after acclimation differed from those with the coexistence of glucose and peptone. The quinone profiles in the acclimation showed that Brevibacterium sp. and Pseudomonas aeruginosa, of which the predominant quinone of the respiratory chain is menaquinone-8(H2) and ubiquinone-9, respectively, multiplied selectively in the acclimation course without and with the coexistence of glucose and peptone, respectively. It was also made clear that there were few kinds and number of protozoa and metazoa in the biofilter treating the wastewater containing AN.

Ionic Liquid Assisted Synthesis of Some 2-Aminobenzenethiols

2019 ◽  
Vol 16 (7) ◽  
pp. 550-555
Author(s):  
Dinesh K. Jangid ◽  
Keshav L. Ameta ◽  
Surbhi Dhadda ◽  
Anjali Guleria ◽  
Prakash G. Goswami ◽  
...  
Keyword(s):  
Ionic Liquid ◽  
Ionic Liquids ◽  
Comparative Study ◽  
Maximum Yield ◽  
Efficient Synthesis ◽  
Target Molecules ◽  
Presence And Absence

Ionic Liquid assisted efficient synthesis of some 2-aminobenzenethiols has been reported using three different Ionic Liquids (ILs) namely methylimidazolium tetrafluoroborate [MIM]+[BF4]−, methylimidazolium chloride [MIM]+[Cl]− and methylimidazolium nitrate [MIM]+[NO3]−. A comparative study has been carried out for the synthesis of target molecules in the presence and absence of IL, leading to conclusion that maximum yield has been observed with [MIM]+[BF4]−.

Dispersive Liquid-Liquid Microextraction Based on Ionic Liquid and Spectrophotometric Determination of Bilirubin in Biological Samples

2020 ◽  
Vol 16 (5) ◽  
pp. 652-659
Author(s):  
Asiye A. Avan ◽  
Hayati Filik
Keyword(s):  
Ionic Liquid ◽  
Ionic Liquids ◽  
Biological Samples ◽  
Urine Samples ◽  
Spectrophotometric Detection ◽  
Full Color ◽  
Dispersive Liquid Liquid Microextraction ◽  
Urine And Serum ◽  
Liquid Microextraction

Background: An Ionic Liquid-based based Dispersive Liquid-Liquid Microextraction (IL-DLLME) method was not applied to preconcentration and determination of bilirubin. Ionic Liquids (ILs) are new chemical compounds. In recent years, Ionic Liquids (ILs) have been employed as alternative solvents to toxic organic solvents. Due to these perfect properties, ILs have already been applied in many analytical extraction processes, presenting high extraction yield and selectivity for analytes. Methods: In this study, IL-DLLME was applied to biological samples (urine and serum) for the spectrophotometric detection of bilirubin. For bilirubin analysis, the full-color development was based on the reaction with periodate in the presence of hydrochloric acid. The high affinity of bilirubin for the ionic liquid phase gave extraction percentages above 98% in 0.3 M HCl solution. Results: Several IL-extraction parameters were optimized and room temperature ionic liquid 1-butyl- 1-methylpyrrolidinium bis(trifluoromethylsulfonyl)imide and ethanol were used as extraction and disperser solution. The linear range was found in the range of 0.5-6.0 μM (0.3-3.5 μg mL-1) and the limits of detection of the proposed method was 0.5 μM (0.3 μg mL-1). The proposed method was applied for the preconcentration and separation of trace bilirubin in real urine samples. Also, the recoveries for bilirubin in spiked biological samples (urine and serum) were found to be acceptable, between 95-102%. Conclusion: The proposed IL-DLLMEapproach was employed for the enrichment and determination of trace levels of bilirubin in urine samples using NaIO4 as an oxidizing agent and Uv-vis spectrophotometric detection. The periodate oxidation of bilirubin is rapid, effective, selective, and simple to perform. The method contains only HCl, NaOI4, and an anionic surfactant. The method may be useful for economizing in the consumption of reagents in bilirubin determining. The IL-DLLMEmethod ensures a high yield and has a low toxicity no skin sensitization, no mutagenicity and no ecotoxicity in an aquatic environment since only very low quantities of an IL is required. For full-color formation, no any extra auxiliary reagents are required. Besides, the IL-DLLME technique uses a low-cost instrument such as Uv-vis which is present in most of the medical laboratories.

Sign in / Sign up

Export Citation Format

Share Document