Selective removal of heavy metal ions using sol-gel immobilized and SPE-coated thiacrown ethers

作者:Saad B*; Chong CC; Ali ASM; Bari MF; Ab Rahman I; Mohamad N; Saleh MI
来源:Analytica Chimica Acta, 2006, 555(1): 146-156.
DOI:10.1016/j.aca.2005.08.070

摘要

Sorbent materials based on three thiacrown ethers, 1,4,7,10-tetrathiacyclododecane (12S4), 1,4,7,10,13-pentathiacyclopentadecane (15S5) and 1,4,7,10.13,16-hexathiacyclooctadecane (18S6) were prepared either by immobilizing the ligands into sol-gel (SG) matrix or coating on commercial solid phase extraction (SPE) column. SG sorbents were characterized by FT-IR, energy dispersive X-ray microanalysis (EDX) and thermogravimetric analysis/derivative thermogravimetric analysis (TGA/DTG). A marked thermal stability of the ligands when immobilized in sol-gel matrix was noted. The competitive sorption characteristics of a mixture of eleven metal ions (Mg2+, Zn2+, Cd2+, Co2+, Mn2+, Ca2+, Cu2+, Ni2+, Ag+, V4+, Hg2+) using: (i) batch method with ligands trapped in SG matrices, and (ii) off-line SPE column containing coated ligands were studied using ICP-MS. The extraction of metals were optimized for key parameters such as pH, contact time/flow rate, particle size (for SG sorbents) and ligand concentration. Under the optimized conditions, all the immobilized thiacrown ethers exhibited highest selectivity toward Ag+, with lesser responses to Hg2+ while the extraction of other metal ions were negligible. Among the SG sorbents, 18S6-SG offer the highest capacity and the best selectivity over Hg2+. However, for practical applications such as for selective isolation and preconcentration of Ag+, the SPE type especially based on 18S6 is preferred as analysis time and recoveries are favorable. The sorbents can be repeatedly used three times as there was no significant deterioration in the metal uptake (%E > 90%) or interference from other metal ions. The optimized procedures were successfully applied for the separation and preconcentration of traces Ag+ in different water samples.

  • 出版日期2006-1-5