A novel sorbent ZIF-67/LDH@C was synthesised using mild etching and co-precipitation and carbonization calcination for the elimination of lead ions (Pb²⁺), malachite green (MG), and congo red (CR) from water. The three-dimensional hollow MOF structure and two-dimensional LDH nanosized layers of ZIF-67/LDH@C were demonstrated by scanning electron microscope (SEM), transmission electron microscopy (TEM), fourier transform infrared (FT-IR), X-ray diffraction (XRD), nitrogen adsorption/desorption, thermogravimetric analysis (TGA), and X-ray photoelectron spectroscopy (XPS) characterization. The maximal adsorption capability of Pb²⁺, MG, and CR could reach 662.25, 1729.83 and 526.32 mg∙g⁻¹, respectively. The kinetic study proved that the adsorption was chemisorption or strong complexation and the rate-limiting step was intraparticle diffusion. The isotherms effectively indicated the monomolecular-type adsorption. Thermodynamic studies showed the spontaneous and endothermic nature of Pb²⁺, MG and CR adsorption onto ZIF-67/LDH@C. The adsorption mechanisms of ZIF-67/LDH@C may be attributed to electrostatic attraction, π-π interaction, hydrogen-bonding interaction, and surface complexation between ZIF-67/LDH@C and pollutants. Furthermore, favourable stability and negligible interference from other metal ions could promote the viability of the practical application of ZIF-67/LDH@C in wastewater purification. Graphical Abstract

In order to realize the effective separation of palladium from high-level liquid waste (HLLW), a ligand-supported adsorbent (NTAamide(C8)/SiO₂-P) was prepared by the impregnation method in a vacuum. The SiO₂-P carrier was synthesized by in situ polymerization of divinylbenzene and styrene monomers on a macroporous silica skeleton. The NTAamide(C8)/SiO₂-P adsorbent was fabricated by impregnating an NTAamide(C8) ligand into the pore of a SiO₂-P carrier under a vacuum condition. The adsorption performance of NTAamide(C8)/SiO₂-P in nitric acid medium has been systematically studied. In a solution of 0.2 M HNO₃, the distribution coefficient of Pd on NTAamide(C8)/SiO₂-P was 1848 mL/g with an adsorption percentage of 90.24%. With the concentration of nitric acid increasing, the adsorption capacity of NTAamide(C8)/SiO₂-P decreases. Compared to the other 10 potential interfering ions in fission products, NTAamide(C8)/SiO₂-P exhibited excellent adsorption selectivity for Pd(II). The separation factor (SF_{Pd/other metals} > 77.8) is significantly higher than that of similar materials. The interference of NaNO₃ had a negligible effect on the adsorption performance of NTAamide(C8)/SiO₂-P, which maintained above 90%. The adsorption kinetics of Pd(II) adsorption on NTAamide(C8)/SiO₂-P fits well with the pseudo-second order model. The Sips model is more suitable than the Langmuir and Freundlich model for describing the adsorption behavior. Thermodynamic analysis showed that the adsorption of Pd(II) on NTAamide(C8)/SiO₂-P was a spontaneous, endothermic, and rapid process. NTAamide(C8)/SiO₂-P also demonstrated good reusability and economic feasibility.

In this study, a novel organic–inorganic hybrid material IIGK@MnO₂ (2-naphthalenemethyl-isoleucine-isoleucine-glycine-lysine@manganese dioxide) was designed as a novel adsorbent for the removal of strontium ions (Sr²⁺). The morphology and structure of IIGK@MnO₂ were characterized using TEM, AFM, XRD, and XPS. The results indicate that the large specific surface area and abundant negative surface charges of IIGK@MnO₂ make its surface rich in active adsorption sites for Sr²⁺ adsorption. As expected, IIGK@MnO₂ exhibited excellent adsorbing performance for Sr²⁺. According to the adsorption results, the interaction between Sr²⁺ and IIGK@MnO₂ can be fitted with the Langmuir isotherm and pseudo-second-order equation. Moreover, leaching and desorption experiments were conducted to assess the recycling capacity, demonstrating significant reusability of IIGK@MnO₂.

Three amphiphilic peptides with varied molecular hydrophobicity, charge number and charge location have been designed as regulators to modulate the crystal growth of zeolitic imidazolate framework-8 (ZIF-8). All three peptides can interact with ZIF-8 to inhibit {100} facet growth and produce truncated cubic crystals. The peptide’s molecular hydrophobicity plays a dominant role in defining the final morphology and size of the ZIF-8 crystals. The peptides with less charge and higher hydrophobicity can promote nuclei formation and crystal growth to give smaller ZIF-8 crystals. However, the charge located in the center of the molecular hydrophobic region has little effect on the crystal nucleation and growth due to the shielding of its charge by molecular aggregation. The study provides insights into the effect of molecular charge and hydrophobicity on ZIF-8 crystal growth and is helpful for guiding the molecular design for regulating the synthesis of metal-organic framework materials.

The separation of palladium from radioactive waste streams represents a critical aspect of the secure handling and disposal of such hazardous materials. Palladium, in addition to its radioactive nature, holds intrinsic value as a resource. Despite the urgency, prevailing adsorbents fall short in their ability to effectively separate palladium under highly acidic environments. To surmount this challenge, our research has pioneered the development of 1,3,5-tris(4-aminophenyl)benzene-2,5-Bis(methylthio)terephthalaldehyde COF (TAPB-BMTTPA-COF), a novel material distinguished by its remarkable stability and an abundance of sulfur-containing functional groups. Leveraging the pronounced affinity of the soft ligands’ nitrogen and sulfur within its molecular architecture, TAPB-BMTTPA-COF demonstrates an exceptional capability for the selective adsorption of palladium. Empirical evidence underscores the material’s swift adsorption kinetics, with equilibrium achieved in as little as ten minutes, and its broad tolerance to varying acidity levels ranging from 0.1 to 3 M HNO₃. Furthermore, TAPB-BMTTPA-COF boasts an impressive adsorption capacity, peaking at 343.6 mg/g, coupled with high selectivity in 13 interfering ions’ environment and the ability to be regenerated, making it a sustainable solution. Comprehensive analyses, including Fourier Transform Infrared Spectroscopy (FT-IR) and X-ray photoelectron spectroscopy (XPS), alongside Density Functional Theory (DFT) calculations, have corroborated the pivotal role played by densely packed nitrogen and sulfur active sites within the framework. These sites exhibit a robust affinity for Pd(II), which is the cornerstone of the material’s outstanding adsorption efficacy. The outcomes of this research underscore the immense potential of COFs endowed with resilient linkers and precisely engineered functional groups. Such COFs can adeptly capture metal ions with high selectivity, even in the face of severe environmental conditions, thereby paving the way for the more effective and environmentally responsible management of radioactive waste.