Room-temperature ionic liquids volatility

Recently, room-temperature ionic liquids (molten salts) have been extensively studied in order to replace volatile organic solvents by them in electrochemical devices such as batteries. Interest in these materials is stimulated by their properties (e.g., high ionic conductivity, good electrochemical stability, and low volatility). Among these properties, the low volatility is the most critical for ensuring the long-term stability of electrochemical devices. Room-temperature ionic liq-... 

Because of its high reactivity (—1.67 V vs. NHE), the electrodeposition of aluminum from aqueous solutions is not possible. Therefore, electrolytes for A1 deposition must be aprotic, such as ionic liquids or organic solvents. The electrodeposition of aluminum in organic solutions is commercially available (SIGAL-process [56, 57]) but due to volatility and flammability there are some safety issues. Therefore, the development of room-temperature ionic liquids in recent years has resulted in another potential approach for aluminum electrodeposition. Many papers have been published on the electrodeposition of aluminum from chloroaluminate (first... 

Room-temperature ionic liquids are the promising electrolytes for the electrodeposition of various metals because they have the merits of both organic electrolytes and high-temperature molten salts. Ionic liquids can be used in a wide temperature range, so temperatures can be elevated to accelerate such phenomena as nucleation, surface diffusion and crystallization associated with the electrodeposition of metals. In addition the process can be safely constracted because ionic liquids are neither flammable nor volatile if they are kept below the thermal decomposition temperature of the organic cations. 

Ionic liquids can be used as replacements for many volatile conventional solvents in chemical processes see Table A-14 in the Appendix. Because of their extraordinary properties, room temperature ionic liquids have already found application as solvents for many synthetic and catalytic reactions, for example nucleophilic substitution reactions [899], Diels-Alder cycloaddition reactions [900, 901], Friedel-Crafts alkylation and acylation reactions [902, 903], as well as palladium-catalyzed Heck vinylations of haloarenes [904]. They are also solvents of choice for homogeneous transition metal complex catalyzed hydrogenation, isomerization, and hydroformylation [905], as well as dimerization and oligomerization reactions of alkenes [906, 907]. The ions of liquid salts are often poorly coordinating, which prevents deactivation of the catalysts. 

Room temperatures ionic liquids (ILs)- salts with melting points below 100°C- have attracted considerable attention as novel reaction media over the last decade. By virtue of their nonflammability, thermal stability and non-volatility ionic liquids have been proposed as alternative solvents receiving serious consideration with the promise of both environmental and technological benefits. Really, recent data showing that commonly used ILs have very low but not null vapour pressures (they can distilled at low pressure), that a large group of ILs is combustible" and some commercially available ionic compoimds are toxic for some aquatic species, have cast a shadow on the "green character of ILs. The instinctive skepticism toward... 

The Friedel-Crafts alkylation of aromatic compounds is of great importance in laboratory synthesis and industrial production. For example, the industrial processes for ethylbenzene, cumene and linear alkylbenzenes, etc., are on the base of this kind of reaction. It is well known that the drawbacks of the traditional acid catalysts such as A1Q3, H SO, and HF do great harm to the equipment and the environment, and these catalysts cannot be reused after the usual aqueous work-up besides, most of the reactions are carried out in the harmful and volatile organic solvents which can cause the environmental pollution aU of these problems need the replacement of the solvents or the acid catalysts. In this context, room-temperature ionic liquids have been iuCTeasingly employed as green solvents. 

Room Temperature Ionic Liquids (RTILs) Versus Volatile Organic Compounds (VOCs) in Organic Electrosynthesis The Requirement of a Careful Comparison... 

Abstract The possible utilization of room temperature ionic liquids (RTILs), instead of volatile organic compounds (VOCs), in the electrochemical procedures of organic synthesis has been discussed. The synthesis of p-lactams, the activation of carbon dioxide and its utilization as renewable carbon source and the carbon-carbon bond formation reactions via umpolung of aldehydes (benzoin condensation and Stetter reaction) and via Henry reaction have been selected as typical electrochani-cal methodologies. The results, related to procedures performed in RTILs, have been compared with those performed in VOCs. The double role of RTILs, as green solvents and parents of electrogenerated reactive intermediates or catalysts, has been emphasized. 

Room Temperature Ionic Liquids (RTILs) Versus Volatile Organic Compounds... 

Chiarotto I, Feroci M, Orsini M, Feeney MMM, Inesi A (2010) Study on the reactivity of aldehydes in electrolysed ionic liquids. Benzoin condensation VOCs (volatile organic compounds) vs RTlLs (room temperature ionic liquids). Adv Synth Catal 352 3287-3292... 

Chapter 16 outlines the possible utihzation of room-temperature ionic liquids (RTILs), instead of volatile organic compounds (VOCs), in the electrochemical procedures of organic synthesis of alpha- and beta-lactams. The activation of carbon dioxide and its utilization as a renewable carbon source is also highlighted. 

Room temperature ionic liquids (RTILs) are molten salts whose melting points are below room temperature. RTILs are formed when the constituent ions are sterically mismatched, thereby hindering crystal formation [17]. As polar solvents, RTILs have unique applications as tunable and environmentally benign solvents with very low volatility, high fire resistance, excellent chemical and thermal stability and wide liquid temperature range and electrochemical windows [17-19]. Solvent applications of RTILs include, for example, organic synthesis [17,20, 21], separations [22, 23], storage and transportation of hazardous chemicals [24], polymeric electrolytes [25, 26], dissolution of natural products [27] and synthesis of hollow metal oxide microspheres [28]. 

---