4.7 Article

Synthesis of a magnetic nanomaterial with core-shell structure for effective Au(III) recovery from solution with superior separation and one-step reduction

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 468, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2023.143750

Keywords

Magnetic nanomaterial; Au(III) recovery; Sorption selectivity; Reduction

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In this study, a magnetic nanomaterial with a core-shell structure was successfully synthesized for effective adsorption of gold ions. The material demonstrated excellent selectivity, one-step reduction, and easy separation, marking a significant breakthrough in the field of gold ion recovery.
To synthesize a novel magnetic nanomaterial for effective Au(III) recovery from the aqueous phase with excellent capability, superior selectivity, one-step reduction and ease of separation after loading Au(III) still remains a huge challenge. In this study, a magnetic nanomaterial (gamma-Fe2O3@PDA-NAM) with a core-shell structure was synthesized for effective Au(III) recovery by sorption. The maximum Au(III) sorption capacity by gamma-Fe2O3@PDA-NAM reached 2910 mg/g at pH = 6.10 +/- 0.15, 44.29 times that by gamma-Fe2O3 (65.7 mg/g). Its Au(III) sorption efficiency was over 97.75% at very low concentrations (i.e., 5.5 x 10-4 and 5.5 x 10-5 mg/mL). TEM, XPS and FTIR analysis verified that excellent Au(III) recovery by gamma-Fe2O3@PDA-NAM resulted from N/S-containing soft base moieties introduced to different layers. N and/or S elements at these sites provided lone pair electrons to Au (III) to form stable coordination bond. Meanwhile, the hydrogen bond between O-containing (-OH,-C=O) and N-containing (-C-N, -N(-C)-N-,-C=N) moieties on gamma-Fe2O3@PDA-NAM and -OH on the main speciations of Au(III) (AuCl3(OH)-, AuCl2(OH)2-, and AuCl(OH)3-) also greatly enhanced Au(III) recovery. About 78.03% of Au(III) was directly reduced to elemental gold by -C-S-and-N(-C) -N-group on the tertiary amine structure during sorption. More than 98.84% of Au(III) was selectively sorbed on gamma-Fe2O3@PDA-NAM at pH 4.0 even though Pt(IV), Cu(II), Zn(II), Pb(II), and Ni(II) were co-present at the same concentration as that for Au(III) (0.01 mg/mL). In contrast, sorption efficiency of other interfering ions was within 1.75-26.05%. A relatively poor sorption selectivity for Pt (IV) could be acceptable because it is also a noble metal.

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