Related Experiment Video
Updated: Nov 14, 2025

Synthesis of High Purity Nonsymmetric Dialkylphosphinic Acid Extractants
Published on: October 19, 2017
Study on Extraction Separation of Thioarsenite Acid in Alkaline Solution by -Type Tri-n-Octylmethyl-Ammonium Chloride
Kang Yan1, Liping Liu1, Hongxing Zhao1
1School of Metallurgical Engineering, Jiangxi University of Science and Technology, Ganzhou, China.
Abstract:
To overcome the problem of arsenic separation and enrichment from an alkaline leaching solution in arsenic-containing dust, a -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 -type by treating organic phase with saturated NaHCO3five times. TOMAC was effectively transformed from to 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% -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%.
More Related Videos
Related Concept Videos
Extraction: Advanced Methods
Preparation and Reactions of Thiols
Preparation of Acid Anhydrides
The carboxylate ion acts as a nucleophile that attacks the carbonyl carbon of the acid chloride to form a tetrahedral intermediate. Subsequently, the re-formation of the carbonyl group with the loss of the chloride ion as a leaving group leads to the formation of an acid...
Acid Halides to Carboxylic Acids: Hydrolysis
As shown below, the mechanism involves a nucleophilic attack by water at the carbonyl carbon to form a tetrahedral intermediate. This is followed by the reformation of the carbon–oxygen π bond along with the departure of a halide ion. A final proton transfer step yields carboxylic...
Qualitative Analysis
For instance, group IV...
Reduction of Alkynes to trans-Alkenes: Sodium in Liquid Ammonia
When dissolved in liquid ammonia, an alkali metal, such as sodium,...

