Bait-and-Anchor Strategy in Dual N/Se-Engineered Resins for Electrostatic-Chelation Cascade Pd(II) Recovery from Extreme Environments

Abstract

The imperative to selectively recover palladium from complex secondary sources is compounded by the significant technical challenges involved. This study introduces a heteroatom-engineered resorcinol-formaldehyde resin microsphere (Se-RF) with dual N/Se doping, which implements a " bait-and-anchor " strategy for highly efficient Pd(II) recovery from challenging environments. The Se-RF adsorbent significantly outperforms conventional RF resins, owing to its heteroatomcooperative capture mechanism. The breakthrough lies in: (1) an ultrafast in situ doping polymerization process, facilitated by high-speed stirring, yielding uniform microspheres within 5 min under ambient conditions; (2) the dual role of ammonia as both polymerization catalyst and nitrogen precursor, creating "soft base" sites that enhance electrostatic affinity; and(3) synergistic N/Se binding, endowing the resin with a high Pd(II) uptake capacity of 447 mg/g at 318 K and 96.65% recovery efficiency from real waste catalyst leachates, with minimal capacity loss (<5%) over five cycles-far surpassing commercial resins (<40%). In situ FTIR, XPS, Raman, and DFT analyses confirm a cascade capture mechanism: protonated N sites act as electrostatic "bait" for preconcentrating [PdCl₄] 2-, while Se sites serve as a strong "anchor" via Pd←N to Pd-Se coordination, enabling effective charge transfer and stable chelation. This work provides a cost-effective and sustainable adsorbent design strategy for precious metal recovery and environmental remediation.

Article information

Article type
Paper
Submitted
20 Nov 2025
Accepted
04 Jan 2026
First published
05 Jan 2026

Green Chem., 2026, Accepted Manuscript

Bait-and-Anchor Strategy in Dual N/Se-Engineered Resins for Electrostatic-Chelation Cascade Pd(II) Recovery from Extreme Environments

F. Wu, H. Li, C. Zheng, Y. Huang and J. Pan, Green Chem., 2026, Accepted Manuscript , DOI: 10.1039/D5GC06228D

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