A customized MOF-polymer composite for rapid gold extraction from water matrices.

With the fast-growing accumulation of electronic waste and rising demand for rare metals, it is compelling to develop technologies that can promotionally recover targeted metals, like gold, from waste, a process referred to as urban mining. Thus, there is increasing interest in the design of materials to achieve rapid, selective gold capture while maintaining high adsorption capacity, especially in complex aqueous-based matrices. Here, a highly porous metal-organic framework (MOF)-polymer composite, BUT-33-poly(para-phenylenediamine) (PpPD), is assessed for gold extraction from several matrices including river water, seawater, and leaching solutions from CPUs. BUT-33-PpPD exhibits a record-breaking extraction rate, with high Au3+ removal efficiency (>99%) within seconds (less than 45 s), a competitive capacity (1600 mg/g), high selectivity, long-term stability, and recycling ability. Furthermore, the high porosity and redox adsorption mechanism were shown to be underlying reasons for the material's excellent performance. Given the accumulation of recovered metallic gold nanoparticles inside, the material was also efficiently applied as a catalyst.

Magnetite drives self-dechlorination of 4-chlorophenol in anoxic aquatic sediments.

The lack of available electron donors is well known as a major factor limiting the efficiency of microbial dechlorination of 4-chlorophenol (4-CP) in anoxic aquatic sediments. Considering that Fe(III) minerals largely contained in sediments can especially enrich Fe(III)-reducing bacteria and unlock the ring-like intermediates produced by dechlorination of 4-CP via dissimilatory Fe(III) reduction, a strategy of self-dechlorination of 4-CP utilizing its metabolism intermediates such as short-fatty acids (SCFAs) as the endogenous electron donors with magnetite was proposed in this study. The results showed that the removal efficiency of 4-CP increased by 156-203% in magnetite-supplemented biotic groups compared with the magnetite-free biotic group. Liquid chromatography-mass spectrometer (LC-MS) and gas chromatography (GC) revealed the possible metabolic pathway of anoxic 4-CP degradation with magnetite: 4-CP→phenol→cyclohexene-1-carboxylic acid→2-hydroxycyclohexanecarboxylic acid→hexanoic acid/valeric acid→butyric/propionic acids→CO2. High-throughput sequencing analysis showed that the abundance of functional bacteria, Desulfuromonas, Pseudomonas and Bacillus species, were increased by 1.38-1.97, 1.50-2.04, and 11.60-17.18 folds in magnetite-supplemented biotic groups, compared with the magnetite-free biotic groups. Analysis of Fe2+ concentration and cyclic voltammetry (CV) suggested that the potential Fe(III)/Fe(II) transformation occurred and proceeded the anoxic 4-CP degradation continuously.