4.7 Article

Highly efficient removal of glyphosate from water by hierarchical-pore UiO-66: Selectivity and effects of natural water particles

期刊

JOURNAL OF ENVIRONMENTAL MANAGEMENT
卷 316, 期 -, 页码 -

出版社

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.jenvman.2022.115301

关键词

Hierarchical-pore; UiO-66(Zr); Glyphosate; Adsorption

资金

  1. National Natural Science Foundation of China [21806001]
  2. Provincial Innovation Training program for College students [S202110364106]

向作者/读者索取更多资源

This study achieved the selective removal of glyphosate from water environments using hierarchical-pore metal-organic framework materials. The materials exhibited high adsorption capacity and suitable selective adsorption performance, allowing for rapid and effective removal of glyphosate in complex aqueous environments.
The selective removal of glyphosate (GP) from aqueous environments is crucial for ensuring human health and environmental sustainability. The preparation of hierarchical-pore MOFs and the reasonable regulation of the pore size are effective strategies for achieving selective removal. In this study, we applied hierarchical-pore UiO66 analogues (HUiO-66s) synthesized by the template technique through a mild method for the removal of GP from water. The results showed that the maximum adsorption capacity of HUiO-66s was as high as 400 mg/g, which is higher than that of most reported adsorbents. Notably, HUiO-66s showed the highest adsorption rate and distribution coefficient for GP in a multivariate system containing different organophosphorus pesticides and antibiotics, exhibiting suitable selective adsorption performance for GP. Furthermore, GP adsorption onto HUiO66-2 (prepared from 2 mL of MOF-5 template) did not affect the presence of competing anions and humic acids. Naturally occurring particles in the water body had an enhanced (i.e., Al2O3, sepiolite, and montmorillonite), reduced (i.e., illite and SiO2), or insignificant (i.e., kaolin) effect on the GP adsorption rate of HUiO-66-2. Further analysis based on the bulk adsorption results and microscopic characterisation indicated that the pore structure synergistically occurred with metal-ligand bonding, hydrogen bonding, and electrostatic interactions, which together determined the GP adsorption. Overall, the high adsorption and apparent adsorption selectivity of HUiO-66s facilitated the rapid separation and removal of GP in complex aqueous environments. Our findings provide insights into the transport and fate of MOFs and contaminants in natural aquatic systems.

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