{"title":"Development of Novel Protic Ionic Liquid Gels Applied for CO<sub>2</sub> Separation Materials","authors":"Kenta Matsumoto, Takeru Sunada, Yuki Murata, Tomohiro Yoshida, Yuki Morita, H. Okamoto","doi":"10.2355/tetsutohagane.tetsu-2023-109","DOIUrl":null,"url":null,"abstract":"Ionic liquids are salts, and their melting points were less than 100 ºC under atmospheric pressure. In particular, ionic liquids, which melting point of them were less than room temperature under atmospheric pressure, have been researched in recent decades. Ionic liquids are well-known to designer’s solvents since configuration of cation and anion are easily to change then specificity is exhibited. In this work, novel protic ionic liquids (PILs) which are applied for CO2 sorption materials have been synthesized using aromatic amine such as alkylpyridine derivatives and N,N-dimethylaniline and bis (trifluoromethanesulfonyl) amide due to co-existing proton conductivity and hydrophobicity. Synthesized PILs exhibited hydrophobicity since 1-octanol–water partition coefficients were more than 0. Also, their ionic conductivities were approximately 10−3 S cm−1 at room temperature, and their mechanism of ionic conduction were different one compared with general electrolyte solution due to high viscosities. In addition, several PILs were high selectivity for CO2 sorption compared with N2. Furthermore, PILs gelatinized with bis[4-(1H,1H,2H,2H-tridecafluorooctyl)phenyl] terephthalates due to improvement of mobility. Some of gel–sol transition temperatures of 5 wt% gels were approximately 100 ºC. The driving force of gelation with ionic liquids might be an entropy driven. Sorption selectivity for CO2 and N2 were similar one before and after gelation.","PeriodicalId":22340,"journal":{"name":"Tetsu To Hagane-journal of The Iron and Steel Institute of Japan","volume":"110 7","pages":"558-567"},"PeriodicalIF":0.4000,"publicationDate":"2024-03-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.jstage.jst.go.jp/article/tetsutohagane/110/7/110_TETSU-2023-109/_pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Tetsu To Hagane-journal of The Iron and Steel Institute of Japan","FirstCategoryId":"0","ListUrlMain":"https://doi.org/10.2355/tetsutohagane.tetsu-2023-109","RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"METALLURGY & METALLURGICAL ENGINEERING","Score":null,"Total":0}
引用次数: 0
Abstract
Ionic liquids are salts, and their melting points were less than 100 ºC under atmospheric pressure. In particular, ionic liquids, which melting point of them were less than room temperature under atmospheric pressure, have been researched in recent decades. Ionic liquids are well-known to designer’s solvents since configuration of cation and anion are easily to change then specificity is exhibited. In this work, novel protic ionic liquids (PILs) which are applied for CO2 sorption materials have been synthesized using aromatic amine such as alkylpyridine derivatives and N,N-dimethylaniline and bis (trifluoromethanesulfonyl) amide due to co-existing proton conductivity and hydrophobicity. Synthesized PILs exhibited hydrophobicity since 1-octanol–water partition coefficients were more than 0. Also, their ionic conductivities were approximately 10−3 S cm−1 at room temperature, and their mechanism of ionic conduction were different one compared with general electrolyte solution due to high viscosities. In addition, several PILs were high selectivity for CO2 sorption compared with N2. Furthermore, PILs gelatinized with bis[4-(1H,1H,2H,2H-tridecafluorooctyl)phenyl] terephthalates due to improvement of mobility. Some of gel–sol transition temperatures of 5 wt% gels were approximately 100 ºC. The driving force of gelation with ionic liquids might be an entropy driven. Sorption selectivity for CO2 and N2 were similar one before and after gelation.
离子液体是盐,在常压下熔点小于100℃。特别是在大气压下熔点低于室温的离子液体,近几十年来得到了广泛的研究。离子液体是设计溶剂所熟知的,因为阳离子和阴离子的结构很容易改变,从而表现出特异性。本研究以烷基吡啶衍生物、N,N-二甲苯胺和双(三氟甲烷磺酰)酰胺等芳香胺为原料,利用其共存的质子导电性和疏水性,合成了用于CO2吸附材料的新型质子离子液体(PILs)。由于1-辛醇-水分配系数大于0,合成的pil具有疏水性。在室温下,它们的离子电导率约为10−3 S cm−1,并且由于它们的高粘度,它们的离子电导率机制与一般电解质溶液不同。此外,与N2相比,几种pil对CO2的吸附选择性较高。此外,由于迁移率的提高,药丸与双[4-(1H,1H,2H,2H-三氟辛基)苯基]对苯二甲酸酯凝胶化。一些5 wt%凝胶的凝胶-溶胶转变温度约为100℃。离子液体凝胶化的驱动力可能是熵驱动的。胶凝前后对CO2和N2的吸附选择性基本一致。
期刊介绍:
The journal ISIJ International first appeared in 1961 under the title Tetsu-to-Hagané Overseas. The title was changed in 1966 to Transactions of The Iron and Steel Institute of Japan and again in 1989 to the current ISIJ International.
The journal provides an international medium for the publication of fundamental and technological aspects of the properties, structure, characterization and modeling, processing, fabrication, and environmental issues of iron and steel, along with related engineering materials.
Classification
I Fundamentals of High Temperature Processes
II Ironmaking
III Steelmaking
IV Casting and Solidification
V Instrumentation, Control, and System Engineering
VI Chemical and Physical Analysis
VII Forming Processing and Thermomechanical Treatment
VIII Welding and Joining
IX Surface Treatment and Corrosion
X Transformations and Microstructures
XI Mechanical Properties
XII Physical Properties
XIII New Materials and Processes
XIV Social and Environmental Engineering.