ABSTRACT
New sulfonate-based chiral salts were prepared from amino alcohols and sodium hydroxymethanesulfonate, vinyl sulfonate, or sultone. The synthesis started with different amino acids from the chiral pool and gave the desired products in just four steps. After cation metathesis, the salts were explored as chiral solvating agents (CSAs) in NMR studies. The new chiral ionic liquids (CILs) were successfully able to interact with different chiral guest molecules and formed diastereomeric aggregates. In some cases, baseline separation was observed. The influence of the structural differences in the CIL as well as the structural requirements of the guest molecule is discussed.
ABSTRACT
In the present work experiments for single mineral flotation against LiAlO2 and melilite s.s. were carried out for seven ionic liquids (ILs). From these, IL-1 with an imidazolium cation and a bromide anion and IL-7 with a pyridinium cation and a bromide anion were selected for further flotation experiments (dosage, pH). Flotation experiments were also conducted using naphthenic acid, a conventional flotation fatty acid-based collector, and FS-2, a commercial collector in order to compare the results with ILs. Moreover, the effects of different anions in the ILs on the flotation were evaluated and a significant influence on the hardness of anions was found on the flotation process. Finally, a pre-functionalization was also explored with modified cholesterol derivatives, comparing the effect of cholesterylsulfate and cholesterylphosphate on the flotation of LiAlO2 and melilite s.s. This study is vital for the further optimization of lithium recovery from the pyrometallurgical recycling path of lithium-ion batteries and the flotation of primary minerals such as aluminosilicates.
ABSTRACT
A Knoevenagel based redox-reaction promoted by intramolecular phosphine sources is presented for the first time. The influence of different diketones, aldehydes, bases and acids was investigated. The effects of different substituents were evaluated based on their electronical influence on the diketone structure. With the obtained results a mechanism is proposed, giving information about transition states formed during the reaction, which can lead to different products. This type of an internal redox transformation with a phosphine oxide moiety remaining in the molecule after the redox reaction represents a new type of reaction.
Subject(s)
Phosphines , Catalysis , Ketones/chemistry , Oxidation-Reduction , Phosphines/chemistry , StereoisomerismABSTRACT
In this work froth flotation studies with LiAlO2 (lithium-containing phase) and Melilite solid solution (gangue phase) are presented. The system was optimized with standard collectors and with compounds so far not applied as collectors. Furthermore, the principle of self-assembled monolayers was introduced to a froth flotation process for the first time resulting in excellent yields and selectivities.