Background: Inflammatory bowel disease is an autoimmune disease that affects the gut. T. spiralis larvae (E/S Ags) loaded on calcium-benzene-1,3,5-tricarboxylate metal-organic frameworks (Ca-BTC MOFs) were tested to determine whether they might prevent or cure acetic acid-induced murine colitis. Methods: T. spiralis larvae E/S Ags/Ca-BTC MOFs were used in prophylactic and therapeutic groups to either precede or follow the development of murine colitis. On the seventh day after colitis, mice were slaughtered. The effect of our target antigens on the progress of the colitis was evaluated using a variety of measures, including survival rate, disease activity index, colon weight/bodyweight, colon weight/length) ratios, and ratings for macroscopic and microscopic colon damage. The levels of inflammatory cytokines (interferon-γ and interleukin-4), oxidative stress marker malondialdehyde, and glutathione peroxidase in serum samples were evaluated. Foxp3 T-reg expression was carried out in colonic and splenic tissues. Results: T. spiralis larvae E/S Ags/Ca-BTC MOFs were the most effective in alleviating severe inflammation in murine colitis. The survival rate, disease activity index score, colon weight/length and colon weight/bodyweight ratios, and gross and microscopic colon damage scores have all considerably improved. A large decrease in proinflammatory cytokine (interferon-γ) and oxidative stress marker (malondialdehyde) expression and a significant increase in interleukin-4 and glutathione peroxidase expression were obtained. The expression of Foxp3+ Treg cells was elevated in colonic and splenic tissues. Conclusion: T. spiralis larvae E/S Ags/Ca-BTC MOFs had the highest anti-inflammatory, antioxidant, and cytoprotective capabilities against murine colitis and might be used to develop new preventative and treatment strategies.

Montmorillonite (Mnt), a clay mineral with a nanolayered structure, was combined with an Fe-based metal–organic framework (MOF; MIL-53(Fe)) using an in situ growth technique that yielded a novel eco-friendly clay-based adsorbent (MIL-53(Fe)@Mnt). The adsorbent was characterized by scanning electron microscopy, Fourier-transform infrared spectroscopy, X-ray diffraction, thermogravimetric analysis and N2 gas adsorption. The MIL-53(Fe) particles grew on the surface of the nanolayered Mnt and the MIL-53(Fe) particle size became smaller. The adsorption performance of MIL-53(Fe)@Mnt was investigated by removing methylene blue (MB), and optimization experiments were carried out to study the effects of contact time, pH, initial dye concentration and adsorbent mass on the adsorption processes. The MIL-53(Fe)@Mnt exhibited excellent adsorption capacity for MB, namely 313.7 mg g−1, which was 3.02 times and 3.54 times greater than that of pure Mnt and MIL-53(Fe), respectively. Adsorption was fitted with the Langmuir isotherm model and followed a pseudo-second order kinetic model. The MIL-53(Fe)@Mnt obtained is a low-cost and eco-friendly adsorbing material and might be a candidate for removing dyes during water treatment.

We use density functional theory meta-generalized gradient approximation TPSS + D3(BJ) + U + J calculations to investigate the energetics and geometry of water molecules in the flexible metal-organic framework material Materials of Institut Lavoisier (MIL)-53(Cr) as a function of cell volume. The critical concentration of water to cause the transition from the large pore (lp) to the narrow pore (np) structure is estimated to be about 0.13 water molecule per Cr. At a concentration x = 1 water molecule per Cr, the zero-temperature np and lp configurations each have a hydrogen bond between the H of each framework hydroxyl group and water oxygen (OW). At intermediate volumes, water dimer-like configurations are observed. A concentration x = 1.25 leads to hydrogen bonding between water molecules in the np phase that is absent for x = 1. Our results suggest possible mechanisms for pore closing in hydrated MIL-53(Cr).

Environmental pollution and energy shortages seriously restrict the development of society. Photocatalytic oxidation technology can directly use solar energy to drive a series of chemical reactions. It has the advantages of low energy consumption, mild reaction conditions, and no secondary pollution, and is an effective method to solve organic pollutions in water. The key to achieve this process is to find and design efficient photocatalytic materials. In this paper, a novel silver-based metal–organic framework (Ag-MOF) [{Ag(H2btc)}{Ag2(Hbtc)}]n (1) (H3btc = 1,3,5-trimesic acid) is designed that exhibits a high performance in the photocatalytic degradation of methylene blue (MB). The process of photocatalytic degradation of MB conforms to pseudo first-order kinetics, and the rate is the fastest at pH 3 (K = 0.2654). Meanwhile, the photocatalytic mechanism of 1 is analyzed by in situ electron paramagnetic resonance (EPR) and ESI-MS spectra. The results are helpful for in situ research of the photocatalytic mechanism of MOFs.

One of the barriers for wide usage of hydrogen energy system is efficient storage. To store more hydrogen efficiently, physisorption is a choice among the others with high storage performance, reversibility, and lifecycles. Metal organic framework (MOF) structured organometallic orotate-Co(II) complexes could serve as sorbents which store hydrogen by physisorption. In this work, mono- and bidentate MOF structured orotate-Co(II) complexes are synthesized, characterized, and then investigated for hydrogen storage experimentally and theoretically. It is found that these compounds could store hydrogen. Especially, the monodentate complex could uptake hydrogen better than the other. Storage performances for mono- and bidentate complexes were 0.80 and 1.15 wt% at 77 K and approximately 80 bars experimentally, 1.03 and 1.16 wt% theoretically for the same conditions.