Modeling the Extraction Rate Coefficient for the Extraction of Yttrium by DEHPA Using Organic-Phase Recycle

2019 ◽  
Vol 37 (6) ◽  
pp. 422-434
Author(s):  
Dave DeSimone ◽  
Natasha Ghezawi ◽  
Thomas Gaetjens ◽  
Robert Counce ◽  
Jack Watson

2021 ◽  
Vol 8 ◽  
Author(s):  
Kang Yan ◽  
Liping Liu ◽  
Hongxing Zhao ◽  
Lei Tian ◽  
Zhifeng Xu ◽  
...  

To overcome the problem of arsenic separation and enrichment from an alkaline leaching solution in arsenic-containing dust, a CO32--type tri-n-octylmethyl-ammonium chloride (TOMAC) method for extracting thioarsenite is proposed in this paper. Considering an alkaline leaching solution as the research object, after vulcanization pretreatment, TOMAC transformation and organic phase saturated extraction capacity were measured, and the extraction mechanism was preliminarily studied. First, Cl−-type quaternary ammonium salt was effectively transformed to HCO3--type by treating organic phase with saturated NaHCO3five times. TOMAC was effectively transformed from HCO3- to CO32- type by alkaline washing with 1.0 mol/l NaOH solution; this washing was repeated thrice. Thereafter, the effects of organic phase composition, phase ratio, extraction time, and temperature on the extraction and separation of arsenic were investigated. The results show that under the conditions of 30% CO32--type TOMAC + 15% sec-octanol + 55% sulfonated kerosene, VO/VA = 1/1, and 5 min extraction at room temperature, the single-stage extraction rate of AsIII is 85.2%. The AsIII concentration in raffinate can be reduced to less than 1.33 × 10−3 mol/l by four-stage countercurrent extraction, and the extraction rate of AsIII can exceed 98.4%.



2013 ◽  
Vol 734-737 ◽  
pp. 1037-1040
Author(s):  
Qing Rong Yang ◽  
Gui Fang Zhang ◽  
Peng Yan

Based on leaching experiments of complex silicate ore contenting scandium, the research has adopted extraction to concentrate scandium and separate impurity. The emphasis of this reaserch is the impact factors, so the experiments including extractant concentration, organic aqueous ratio, mixing time, organic phase washing, organic phase reextraction, have been conducted. The optimal conditions are that the concentration of extraction is 25%, the O/A is 1:10, the mixing time is 3min, the washing time is 3, the O/A of reextraction is 1:2.3, and the extraction rate of exceeding 98% and reextracion rate of 99.01% were obtained when adopting P501 as the extraction agent.





2020 ◽  
Author(s):  
Vishwanath R.S ◽  
Masa-aki Haga ◽  
Takumi Watanabe ◽  
Emilia Witkowska Nery ◽  
Martin Jönsson-Niedziolka

Here we describe the synthesis and electrochemical testing of a heteroleptic bis(tridentate) ruthenium(II) complex [Ru<sup>II</sup>(LR)(L)]<sup>0</sup> (LR =2,6-bis(1-(2-octyldodecan)benzimidazol-2-yl)pyridine, L = 2,6-bis(benzimidazolate)pyridine). It is a neutral complex which undergoes a quasireversible oxidation and reduction at relatively low potential. The newly synthetized compound was used for studies of ion-transfer at the three-phase junction because of the sensitivity of this method to cation expulsion. The [Ru<sup>II</sup>(LR)(L)]<sup>0</sup> shows exceptional stability during cycling and is sufficiently lipophilic even after oxidation to persist in the organic phase also using very hydrophilic anions such as Cl<sup>−</sup>. Given its low redox potential and strong lipophilicity this compound will be of interest as an electron donor in liquid-liquid electrochemistry.



2020 ◽  
Author(s):  
Vishwanath R.S ◽  
Masa-aki Haga ◽  
Takumi Watanabe ◽  
Emilia Witkowska Nery ◽  
Martin Jönsson-Niedziolka

Here we describe the synthesis and electrochemical testing of a heteroleptic bis(tridentate) ruthenium(II) complex [Ru<sup>II</sup>(LR)(L)]<sup>0</sup> (LR =2,6-bis(1-(2-octyldodecan)benzimidazol-2-yl)pyridine, L = 2,6-bis(benzimidazolate)pyridine). It is a neutral complex which undergoes a quasireversible oxidation and reduction at relatively low potential. The newly synthetized compound was used for studies of ion-transfer at the three-phase junction because of the sensitivity of this method to cation expulsion. The [Ru<sup>II</sup>(LR)(L)]<sup>0</sup> shows exceptional stability during cycling and is sufficiently lipophilic even after oxidation to persist in the organic phase also using very hydrophilic anions such as Cl<sup>−</sup>. Given its low redox potential and strong lipophilicity this compound will be of interest as an electron donor in liquid-liquid electrochemistry.



2020 ◽  
Author(s):  
Vishwanath R.S ◽  
Masa-aki Haga ◽  
Takumi Watanabe ◽  
Emilia Witkowska Nery ◽  
Martin Jönsson-Niedziolka

Here we describe the synthesis and electrochemical testing of a heteroleptic bis(tridentate) ruthenium(II) complex [Ru<sup>II</sup>(LR)(L)]<sup>0</sup> (LR =2,6-bis(1-(2-octyldodecan)benzimidazol-2-yl)pyridine, L = 2,6-bis(benzimidazolate)pyridine). It is a neutral complex which undergoes a quasireversible oxidation and reduction at relatively low potential. The newly synthetized compound was used for studies of ion-transfer at the three-phase junction because of the sensitivity of this method to cation expulsion. The [Ru<sup>II</sup>(LR)(L)]<sup>0</sup> shows exceptional stability during cycling and is sufficiently lipophilic even after oxidation to persist in the organic phase also using very hydrophilic anions such as Cl<sup>−</sup>. Given its low redox potential and strong lipophilicity this compound will be of interest as an electron donor in liquid-liquid electrochemistry.



2018 ◽  
Author(s):  
Nam Kyong-il ◽  
KIM rak-chon ◽  
Kang chang-hyok ◽  
Lee song-nam ◽  
Ryom sok-hun

In order to extract lycopene more effectively, this experiment focused on the optimization of ethanol pretreatment method to study the effects of ethanol treatment on the extraction rate of lycopene and its antioxidant activity. The test results show that 2 times ethanol treatment is very effective for improving lycopene yield. The optimum conditions of ethanol treatment are temperature 50 ℃, treatment time 1 time 2h, 2 times 2h, solid to liquid ratio is 1:12. The lycopene yield can be reached 20mg / 100g above.





1979 ◽  
Vol 44 (12) ◽  
pp. 3656-3664
Author(s):  
Oldřich Navrátil ◽  
Jiří Smola ◽  
Rostislav Kolouch

Extraction of hafnium(IV) was studied from solutions of mixtures of perchloric and nitric acids and of perchloric and hydrochloric acids for constant ionic strength, I = 2, 4, 6, or 8, and for cHf 4 . 10-4 mol l-1. The organic phase was constituted by solutions of some acidic or neutral organophosphorus reagents or of 2-thenoyltrifluoroacetone, 1-phenyl-3-methyl-4-benzoyl-5-pyrazolone, or N-benzoyl-N-phenylhydroxylamine in benzene, chloroform, or n-octane. A pronounced synergic extraction of hafnium proceeds only on applying organophosphorus reagents from an aqueous phase whose acidity is not lower than 3M-(HClO4 + HNO3) or 5M-(HClO4 + HCl). The synergic effect was not affected markedly by a variation of the initial concentration of hafnium in the range 1 . 10-8 -4 .10-4 mol l-1, it lowered with increasing initial concentration of the organophosphorus reagent and decreasing concentration of the H+ ions. It is suggested that the hafnium passes into the organic phase in the form of mixed complexes, the salting-out effect of perchloric acid playing an appreciable part.



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