“…Compared to the same carbon numbers, the order of melting points is alcohol > ketone > ester ∼ hydrocarbon > ether, and that of flash points is alcohol > ketone ∼ ester > hydrocarbon ∼ ether. The melting points under 10 o C and flash points over 70 o C are preferable for the use of diluent, therefore, the ranges to use for carbon numbers in diluents are alcohol (8)(9)(10)(11)(12), ketone (9-12), ester (9-12), hydrocarbon (> 10), and ether (> 12). Information is available to show which structure is a useful diluent.…”
Section: Basic Properties Of Diluentsmentioning
confidence: 99%
“…Liquid-liquid extraction methods are also useful for Cs recovery. In this case, crown ether compounds and calix-crown compounds for Cs and Sr extraction are promising [11][12][13][14][15]. The normal crown compounds are generally water-miscible; dibenzo-18crown6 and di-t-butyl-dibenzo-18crown6 are available for Cs extraction because of their lipophilicity and dicyclohexyl-18crown6 and di-t-butyl-dicyclohexyl-18crown6 (DtBuDCH18C6) are also useful for Sr extraction [14,15].…”
High concentration of Cs is present in high-level radioactive waste. It is well-known that Cs is an alkali element and difficult to extract completely into an organic phase. Crown ether compounds are widely available for Cs extractants; DtBuDB18C6 (di-t-butyl-dibenzo-18crown6), was used in this study. Organic solvents used for the industrial applications, such as n-dodecane and 1-octanol, have low solubility concerning the compound; other solvents were employed and tested. In this study, ketone-, ether-, and estertype solvents showed high solubility for DtBuDB18C6 and DtBuDB18C6, when dissolved in ketones and alcohols, exhibited relatively high Cs distribution ratios (D(Cs)), closely to 10.
“…Compared to the same carbon numbers, the order of melting points is alcohol > ketone > ester ∼ hydrocarbon > ether, and that of flash points is alcohol > ketone ∼ ester > hydrocarbon ∼ ether. The melting points under 10 o C and flash points over 70 o C are preferable for the use of diluent, therefore, the ranges to use for carbon numbers in diluents are alcohol (8)(9)(10)(11)(12), ketone (9-12), ester (9-12), hydrocarbon (> 10), and ether (> 12). Information is available to show which structure is a useful diluent.…”
Section: Basic Properties Of Diluentsmentioning
confidence: 99%
“…Liquid-liquid extraction methods are also useful for Cs recovery. In this case, crown ether compounds and calix-crown compounds for Cs and Sr extraction are promising [11][12][13][14][15]. The normal crown compounds are generally water-miscible; dibenzo-18crown6 and di-t-butyl-dibenzo-18crown6 are available for Cs extraction because of their lipophilicity and dicyclohexyl-18crown6 and di-t-butyl-dicyclohexyl-18crown6 (DtBuDCH18C6) are also useful for Sr extraction [14,15].…”
High concentration of Cs is present in high-level radioactive waste. It is well-known that Cs is an alkali element and difficult to extract completely into an organic phase. Crown ether compounds are widely available for Cs extractants; DtBuDB18C6 (di-t-butyl-dibenzo-18crown6), was used in this study. Organic solvents used for the industrial applications, such as n-dodecane and 1-octanol, have low solubility concerning the compound; other solvents were employed and tested. In this study, ketone-, ether-, and estertype solvents showed high solubility for DtBuDB18C6 and DtBuDB18C6, when dissolved in ketones and alcohols, exhibited relatively high Cs distribution ratios (D(Cs)), closely to 10.
“…11 The hydrophobic character of DPA -has been investigated in the ion-pair extraction of DPA -with alkali metal-crown ether complexes. 12,13 The extraction or precipitation characteristics of an alkali metal ion was improved as a crown ether complex, and K + was indirectly determined with DPA -by spectrophotometric flow injection analysis, 14 in which dicyclohexyl-18-crown-6 ether (DC18C6) was used as a complexing reagent for K + and the dissolved concentration of DPA -was decreased by the precipitation formed between K + @DC18C6 and DPA -. 14 Recently, the specific precipitation property of DPA -with K + and Cs + has been investigated by Eringathodi et al 15 based on a crystallographic study of the precipitates.…”
The ion-association equilibrium of the dipicrylaminate ion (DPA -) was investigated in an aqueous solution with alkali metal ions and with its 18-crown-6 ether complexes as pairing cations by capillary zone electrophoresis (CZE). Although DPA -is precipitable with the pairing cations of K + and Cs + in a homogenous aqueous solution, a low concentration of DPA -below its solubility suppressed the formation of the precipitates, and DPA -was detected as a usual CZE signal. Changes in the electrophoretic mobility of DPA -was analyzed for its ion-association equilibrium. The ion association constants determined were almost comparable among alkali metal ions, while the ion association constants were meaningfully large with a hydrophobic 18-crown-6 ether complex of K + . The CZE separation was also proved to be useful for the equilibrium analysis under precipitating conditions. It was suggested that the precipitable property of DPA -with K + and Cs + could not be attributed to the ion-association process in an aqueous solution, but to the condensation process concerning the intermolecular CH···O bond in the precipitate crystals, as reported.Keywords Dipicrylaminate ion, alkali metal ions, 18-crown-6 ether complexes, ion-association equilibrium, aqueous solution, capillary zone electrophoresis
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