The recovery of gold from water is an important research area. Recent reports have highlighted the ultrahigh capacity and selective extraction of gold from electronic waste using reduced graphene oxide (rGO). Here, we made a further attempt with the thermal rGO membranes and found that the thermal rGO membranes also had a similarly high adsorption efficiency (1.79 g gold per gram of rGO membranes at 1000 ppm). Furthermore, we paid special attention to the detailed selectivity between Au³⁺ and other ions by rGO membranes. The maximum adsorption capacity for Au³⁺ ions was about 16 times that of Cu²⁺ ions and 10 times that of Fe³⁺ ions in a mixture solution with equal proportions of Au³⁺/Cu²⁺ and Au³⁺/Fe³⁺. In a mixed-ion solution containing Au³⁺:Cu²⁺:Na⁺:Fe³⁺:Mg²⁺ of printed circuit board (PCB), the mass of Au³⁺:Cu²⁺:Na⁺:Fe³⁺:Mg²⁺ in rGO membranes is four orders of magnitude higher than the initial mass ratio. A theoretical analysis indicates that this selectivity may be attributed to the difference in the adsorption energy between the metal ions and the rGO membrane. The results are conducive to the usage of rGO membranes as adsorbents for Au capture from secondary metal resources in the industrial sector.

The ion-enrichment inside carbon nanotubes (CNTs) offers the possibility of applications in water purification, ion batteries, memory devices, supercapacitors, field emission and functional hybrid nanostructures. However, the low filling capacity of CNTs in salt solutions due to end caps and blockages remains a barrier to the practical use of such applications. In this study, we fabricated ultra-short CNTs that were free from end caps and blockages using ball milling and acid pickling. We then compared their ion-enrichment capacity with that of long CNTs. The results showed that the ion-enrichment capacity of ultra-short CNTs was much higher than that of long CNTs. Furthermore, a broad range of ions could be enriched in the ultra-short CNTs including alkali-metal ions (e.g., K⁺), alkaline-earth-metal ions (e.g., Ca²⁺) and heavy-metal ions (e.g., Pb²⁺). The ultra-short CNTs were much more unobstructed than the raw long CNTs, which was due to the increased orifice number per unit mass of CNTs and the decreased difficulty in removing the blockages in the middle section inside the CNTs. Under the hydrated-cation–π interactions, the ultra-short CNTs with few end caps and blockages could highly efficiently enrich ions.