Abstract
A new diallyl amine salt monomer (I) bearing Li+ chelating 12-Crown-4 ether motifs [(H2C = CHCH2)2NH+CH2-(12-C-4) Cl−] was synthesized. Monomer (I) under free radical cyclopolymerization and alternate copolymerization with SO2 afforded homo (II) and copolymer (III) in good yields. Terpolymerization of I, SO2, and a cross-linker tetraallylhexane-1,6-diammonium chloride (IV) gave cross-linked resin V, which has been utilized as a scavenger for lithium ions from aqueous samples via the liquid‒solid technique. Optimizing a method involves adjusting multiple variables, such as pH, Li+ concentration, and resin dose, to achieve the best possible results. The adsorption capacity was determined using inductively coupled plasma-optical emission spectroscopy (ICP‒OES). The lithium removal study was conducted at concentrations ranging from 20 to 100 ppm. Resin V adsorbs lithium ions rapidly with excellent efficiency following second-order kinetics and fitting the Temkin and Langmuir adsorption isotherms. The resin demonstrated remarkable selectivity in adsorbing Li+ from its binary mixtures Li+/Na+ and Li+/K+.
| Original language | English |
|---|---|
| Article number | 34980 |
| Journal | Scientific Reports |
| Volume | 15 |
| Issue number | 1 |
| DOIs | |
| State | Published - Dec 2025 |
Bibliographical note
Publisher Copyright:© The Author(s) 2025.
Keywords
- 12-Crown-4-ether
- Cyclopolymerization
- Diallyl amine salts
- Lithium ion
- Selective extraction
ASJC Scopus subject areas
- General