Crown ethers as solvent extraction reagents: where do we stand
Conference
·
· Sep. Sci. Technol.; (United States)
OSTI ID:6190185
It is perhaps prophetic that among the first applications of crown ethers was their use as solvent extraction reagents. In 1962 the compound 2,3,11,12-dibenzo- 1,4,7,10,13,16-hexaoxacycloocta-2, 11-diene, now mercifully called dibenzo-18-crown-6, was identified and was found to form alkali-metal-salt adducts that were soluble in organic solvents. These serendipitously discovered extraction properties of crown ethers were later used to compare the complex-formation properties of metal ions with crown ethers, and it was observed that salts of organophilic anions were more readily transferred to aprotic solvents. Picrate salts were extensively used in this role. However, those seeking analytical or process applications of the unusual complexing abilities of macrocycles needed the aqueous anion to be one of the more common mineral acid anions such as chloride, nitrate, or sulfate. This problem was circumvented in the late 1970's when it was discovered that crown ethers mixed with an organophilic cation exchanger such as alkyl phosphoric, alkyl-aryl sulfonic, or carboxylic acid, would produce synergistic extraction systems having excellent and selective affinities for a large number of metal ions. In 1981, macrocyclic compounds with attached carboxylic groups were synthesized and found to be excellent extractants. In addition to liquid-liquid extraction, much work has been done using macrocycles as separation agents in membranes and resin beads. Fundamental research is now beginning to provide the stoichiometries and structures of some of the organic-phase complexes produced and an understanding of the reactions in these extraction systems. At the same time, some potential uses of these systems are beginning to be identified.
- Research Organization:
- Oak Ridge National Lab., TN (USA)
- OSTI ID:
- 6190185
- Report Number(s):
- CONF-871038-
- Conference Information:
- Journal Name: Sep. Sci. Technol.; (United States) Journal Volume: 23:12-13
- Country of Publication:
- United States
- Language:
- English
Similar Records
Crown ethers as solvent extraction reagents: Where do we stand
Size selective synergism by crown ethers in the extraction of alkali metals by di(2-ethylhexyl) phosphoric acid
Solvent extraction of radium with crown ether carboxylic acids
Conference
·
Wed Dec 31 23:00:00 EST 1986
·
OSTI ID:5897067
Size selective synergism by crown ethers in the extraction of alkali metals by di(2-ethylhexyl) phosphoric acid
Conference
·
Mon Dec 31 23:00:00 EST 1979
·
OSTI ID:5104771
Solvent extraction of radium with crown ether carboxylic acids
Journal Article
·
Sat Oct 15 00:00:00 EDT 1994
· Analytical Chemistry (Washington); (United States)
·
OSTI ID:6768349
Related Subjects
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY
38 RADIATION CHEMISTRY, RADIOCHEMISTRY, AND NUCLEAR CHEMISTRY
400105* -- Separation Procedures
400702 -- Radiochemistry & Nuclear Chemistry-- Properties of Radioactive Materials
ALCOHOLS
ALKALI METALS
ALKALINE EARTH METALS
ALKENES
DATA
ELEMENTS
ETHYLENE
EXPERIMENTAL DATA
EXTRACTION
GLYCOLS
HYDROCARBONS
HYDROXY COMPOUNDS
INFORMATION
METALS
NUMERICAL DATA
ORGANIC COMPOUNDS
PH VALUE
RADIUM
SEPARATION PROCESSES
SOLVENT EXTRACTION
SOLVENT PROPERTIES
USES
38 RADIATION CHEMISTRY, RADIOCHEMISTRY, AND NUCLEAR CHEMISTRY
400105* -- Separation Procedures
400702 -- Radiochemistry & Nuclear Chemistry-- Properties of Radioactive Materials
ALCOHOLS
ALKALI METALS
ALKALINE EARTH METALS
ALKENES
DATA
ELEMENTS
ETHYLENE
EXPERIMENTAL DATA
EXTRACTION
GLYCOLS
HYDROCARBONS
HYDROXY COMPOUNDS
INFORMATION
METALS
NUMERICAL DATA
ORGANIC COMPOUNDS
PH VALUE
RADIUM
SEPARATION PROCESSES
SOLVENT EXTRACTION
SOLVENT PROPERTIES
USES