Solvent Extraction of Sodium Permanganate by Mono-benzo 3m-Crown-m Ethers (m = 5, 6) into 1,2-Dichloroethane and Nitrobenzene: a Method which Analyzes the Extraction System with the
Abstract:Analytical equations were derived for the extraction of univalent metal salts (MA) by crown ethers (L) into polar diluents. Then, NaMnO 4 was extracted at 25 C by benzo-15-crown-5 and -18-crown-6 ethers (B15C5 and B18C6) from a water (w)-phase into a 1,2-dichloroethane (DCE)-one. So, the extraction constants of K ex1 and K ex2 were determined, where : distribution constant into NB) values with those previously-reported by other methods, the validity of the equations was confirmed. Additionally, extraction-abi… Show more
“…That is, extraction experiments with M(NO 3 ) 2 , HPic, and 18C6 or DB18C6 were not performed anew. Other procedures for calculation were similar to those (Kudo, Harashima et al, 2011;Kudo, Horiuchi et al, 2013;Kudo, Kobayashi, Katsuta, & Takeda, 2009) described before.…”
Section: Re-calculation Of the Extraction And Other Constants For Thementioning
confidence: 99%
“…Additionally, the extraction of CdBr 2 or CdPic 2 by 18C6 into various diluents with lower polarities, such as Bz, chloroform, dichloromethane, and DCE, has been studied . However, these papers (Kudo, Harashima et al, 2011;Kudo, Horiuchi et al, 2013) did not verify what kind of effect changes of M 2+ and L give on magnitudes of the individual distribution constants (K D,A ) of A .…”
Section: Introductionmentioning
confidence: 99%
“…into DCE and nitrobenzene saturated with water (Kudo et al, 2011). Additionally, the extraction of CdBr 2 or CdPic 2 by 18C6 into various diluents with lower polarities, such as Bz, chloroform, dichloromethane, and DCE, has been studied .…”
Section: Introductionmentioning
confidence: 99%
“…For example, KLPic dissociates into KL + and picrate ion (Pic ) in dichloromethane (Frensdorff, 1971) and water (Takeda, 2002) at L = dibenzo-18-crown-6 ether (DB18C6) and n = 1 and in 1,2-dichloroethane (DCE) at L = 18-crown-6 ether, 18C6, and n = 1 (Kolthoff & Chantooni, 1993); CaLA 2 dissociates into CaLA + and A at L = dicyclohexyl-18C6, A = dipicrylaminate ion, and n = 2 (Jawaid & Ingman, 1978). In solvent extraction, the presence of such equilibria means at least the presence (Kudo, Harashima, Katsuta, & Takeda, 2011;Kudo, Katsuta, & Takeda, 2012;Kudo, Horiuchi, Katsuta, & Takeda, 2013) of the individual distribution of A (or MLA + ) into the organic phase under the condition that the free A (or MLA + ) is detected in the aqueous phase. Furthermore, this distribution is related to an ion transfer of A across a liquid/liquid interface, such as nitrobenzene/aqueous and DCE/aqueous ones, and then its distribution data have been connect with electrochemical properties of A at the interface (Osakai & Ebina, 1998;Kudo & Takeuchi, 2013).…”
Three kinds of extraction constants, K ex , K ex , and K ex+ , were evaluated from the improved model that the following three component-equilibria were added to a previously-proposed model for an overall extraction: M 2+
“…That is, extraction experiments with M(NO 3 ) 2 , HPic, and 18C6 or DB18C6 were not performed anew. Other procedures for calculation were similar to those (Kudo, Harashima et al, 2011;Kudo, Horiuchi et al, 2013;Kudo, Kobayashi, Katsuta, & Takeda, 2009) described before.…”
Section: Re-calculation Of the Extraction And Other Constants For Thementioning
confidence: 99%
“…Additionally, the extraction of CdBr 2 or CdPic 2 by 18C6 into various diluents with lower polarities, such as Bz, chloroform, dichloromethane, and DCE, has been studied . However, these papers (Kudo, Harashima et al, 2011;Kudo, Horiuchi et al, 2013) did not verify what kind of effect changes of M 2+ and L give on magnitudes of the individual distribution constants (K D,A ) of A .…”
Section: Introductionmentioning
confidence: 99%
“…into DCE and nitrobenzene saturated with water (Kudo et al, 2011). Additionally, the extraction of CdBr 2 or CdPic 2 by 18C6 into various diluents with lower polarities, such as Bz, chloroform, dichloromethane, and DCE, has been studied .…”
Section: Introductionmentioning
confidence: 99%
“…For example, KLPic dissociates into KL + and picrate ion (Pic ) in dichloromethane (Frensdorff, 1971) and water (Takeda, 2002) at L = dibenzo-18-crown-6 ether (DB18C6) and n = 1 and in 1,2-dichloroethane (DCE) at L = 18-crown-6 ether, 18C6, and n = 1 (Kolthoff & Chantooni, 1993); CaLA 2 dissociates into CaLA + and A at L = dicyclohexyl-18C6, A = dipicrylaminate ion, and n = 2 (Jawaid & Ingman, 1978). In solvent extraction, the presence of such equilibria means at least the presence (Kudo, Harashima, Katsuta, & Takeda, 2011;Kudo, Katsuta, & Takeda, 2012;Kudo, Horiuchi, Katsuta, & Takeda, 2013) of the individual distribution of A (or MLA + ) into the organic phase under the condition that the free A (or MLA + ) is detected in the aqueous phase. Furthermore, this distribution is related to an ion transfer of A across a liquid/liquid interface, such as nitrobenzene/aqueous and DCE/aqueous ones, and then its distribution data have been connect with electrochemical properties of A at the interface (Osakai & Ebina, 1998;Kudo & Takeuchi, 2013).…”
Three kinds of extraction constants, K ex , K ex , and K ex+ , were evaluated from the improved model that the following three component-equilibria were added to a previously-proposed model for an overall extraction: M 2+
“…− , into various diluents or organic (o) phases have been determined in course of determination of extraction constants (K ex ) for the extraction of some salts, M I A and M II A 2 , by crown compounds (L) [1]- [4]. Here, K D,A and log K = −1.01 1 [6] for the distribution into DCE and +0.05 for that into NB [6].…”
How to cite this paper: Kudo, Y., et al. (2014) − , into the two diluents were also determined with the determination of K ex . From comparison of these K D,Pic values with those standardized, interfacial potential differences (∆φ eq ) at extraction equilibria were evaluated. Then, using these ∆φ eq values, relations of the experimentally-determined logK ex± or logK ex values with their electrochemically-standardized ones were precisely discussed. Consequently, it was indicated that logK ex± should be expressed as a function of ∆φ eq .
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