Adsorption and removal of organophosphorus pesticides from Chinese cabbages and green onions by using metal organic frameworks based on the mussel-inspired adhesive interface.

Based on the mussel-inspired adhesive interface (Fe3O4-g-C3N4@PDA), a novel bionic metal-organic framework (Fe3O4-g-C3N4-PDA@MIL-101) was successfully prepared. The composite featured a high specific surface area and a multi-microchannel structure, as well as strong thermochemical stability. The structural property of Fe3O4-g-C3N4-PDA@MIL-101(Fe) was characterized, and the results indicated that Fe3O4, PDA, and MIL-101(Fe) were uniformly coated on the g-C3N4 surface. The adsorption and desorption of organophosphorus pesticides with Fe3O4-g-C3N4-PDA@MIL-101(Fe) were evaluated by batch experiments. This composite showed high adsorption efficiency and selective removal of coralox, phosalone, and chlorpyrifos. Under the optimal conditions, three organophosphorus pesticides were adsorbed from Chinese cabbage and green onion samples with Fe3O4-g-C3N4-PDA@MIL-101(Fe). The analytical method exhibited high sensitivity (LOD, 0.19-2.34 µg/L; LOQ, 0.65-7.82 µg/L), excellent practicality, and good stability, suggesting that Fe3O4-g-C3N4-PDA@MIL-101 was an ideal candidate magnetic adsorbent for the removal of organophosphorus pesticides in Chinese cabbage and green onion samples.

Tailored metal-organic frameworks facilitate the simultaneously high-efficient sorption of UO22+ and ReO4- in water.

The simultaneously efficient extraction of radioactive metal cations and anions from radioactive waste is of great interest for the proper disposal of spent fuel and environmental protection. Modifying metal-organic frameworks (MOFs) into multifunctional materials with controllable and desired properties is an efficient strategy for broadening their practical applications. Herein, poly(ethyleneimine) (PEI) tailored MIL-101(Cr) (MILP) was obtained through an easy operation and low-cost strategy and was utilized to simultaneously extract uranium (UO22+) and rhenium (ReO4-) from water. The effects of PEI coating amounts, system pH, contact time, initial UO22+/ReO4- concentrations, ionic strength, as well as interfering ions were studied to evaluate the sorption performance of MILP composites. The maximum sorption capacity was 416.67 mg/g for UO22+ at pH 5.5 and 434.78 mg/g for ReO4- at pH 3.5, levels that are superior to those of most adsorbents. The sorption of UO22+/ReO4- occurred in a pH-dependent, spontaneous and endothermic manner, which showed preferable modeling by the pseudo-second-order (PSO) kinetic equation and Freundlich isotherm equation. The adsorption of ReO4- was inhibited by the coexistence of UO22+ and high ion strength. Batch experiments and X-ray photoelectron spectroscopy (XPS) results indicate that UO22+/ReO4- sorption was driven by the abundant amino groups and unsaturated metal sites in the MILP-3 composites. MILP-3 also showed excellent recycling performance and maintained high sorption capacities for UO22+/ReO4- in different simulated water samples. This study shows that MILP composites can effectively extract radioactive metal cations and anions from water, and lays a foundation for designing an excellent new category of candidates with versatile functions for wastewater management.

Synthesis of Nano/Microsized MIL-101Cr Through Combination of Microwave Heating and Emulsion Technology for Mixed-Matrix Membranes.

Nano/microsized MIL-101Cr was synthesized by microwave heating of emulsions for the use as a composite with Matrimid mixed-matrix membranes (MMM) to enhance the performance of a mixed-gas-separation. As an example, we chose CO2/CH4 separation. Although the incorporation of MIL-101Cr in MMMs is well-known, the impact of nanosized MIL-101Cr in MMMs is new and shows an improvement compared to microsized MIL-101Cr under the same conditions and mixed-gas permeation. In order to reproducibly obtain nanoMIL-101Cr microwave heating was supplemented by carrying out the reaction of chromium nitrate and 1,4-benzenedicarboxylic acid in heptane-in-water emulsions with the anionic surfactant sodium oleate as emulsifier. The use of this emulsion with the phase inversion temperature (PIT) method offered controlled nucleation and growth of nanoMIL-101 particles to an average size of <100 nm within 70 min offering high apparent BET surface areas (2,900 m2 g-1) and yields of 45%. Concerning the CO2/CH4 separation, the best result was obtained with 24 wt.% of nanoMIL-101Cr@Matrimid, leading to 32 Barrer in CO2 permeability compared to six Barrer for the neat Matrimid polymer membrane and 21 Barrer for the maximum possible 20 wt.% of microMIL-101Cr@Matrimid. The nanosized filler allowed reaching a higher loading where the permeability significantly increased above the predictions from Maxwell and free-fractional-volume modeling. These improvements for MMMs based on nanosized MIL-101Cr are promising for other gas separations.

Dispersive micro-solid-phase extraction of herbicides in vegetable oil with metal-organic framework MIL-101.

Dispersive microsolid-phase extraction based on metal-organic framework has been developed and applied to the extraction of triazine and phenylurea herbicides in vegetable oils in this work. The herbicides were directly extracted with MIL-101 from diluted vegetables oils without any further cleanup. The separation and determination of herbicides were carried out on high performance liquid chromatography. The effects of experimental parameters, including volume ratio of n-hexane to oil sample, mass of MIL-101, extraction time, centrifugation time, eluting solvent, and elution time were investigated. The Student's t test was applied to evaluate the selected experimental conditions. The limits of detection for the herbicides ranged from 0.585 to 1.04 µg/L. The recoveries of the herbicides ranged from 87.3 to 107%. Our results showed that the present method is rapid, simple, and effective for extracting herbicides in vegetable oils.