A new imidazol-2yl-phosphonic acid/mesoporous silica sorbent (ImP(O)(OH)/SiO) was developed and applied for uranium(VI) ion removal from aqueous solutions. The synthesized material was characterized by fast kinetics and an extra-high adsorption capacity with respect to uranium. The highest adsorption efficiency of U(VI) ions was obtained for the reaction system at pH 4 and exceeded 618 mg/g. The uranium(VI) sorption proceeds quickly in the first step within 60 min of the adsorbent sites and ion interactions. Moreover, the equilibrium time was determined to be 120 min. The equilibrium and kinetic characteristics of the uranium(VI) ions uptake by synthesized sorbent was found to follow the Langmuir-Freundlich isotherm model and pseudo-second-order kinetics rather than the Langmuir, Dubinin-Radushkevich, and Temkin models and pseudo-first-order or intraparticle diffusion sorption kinetics. The adsorption mechanism for uranium on the sorbent was clarified basing on the X-ray photoelectron spectroscopy (XPS) analysis. The model of UO binding to surface of the sorbent was proposed according to the results of XPS, i.e., a 1:1 U-to-P ratio in the sorbed complex was established. The regeneration study confirms the ImP(O)(OH)/SiO sorbent can be reused. A total of 45% of uranium ions was determined as originating from the sorbent leaching in the acidic solutions, whereas when the basic solutions were used, the removal efficiency was 12%.

Download full-text PDF

Source
http://dx.doi.org/10.1021/acsami.7b17594DOI Listing

Publication Analysis

Top Keywords

uraniumvi ion
8
sorbent
7
imidazole-2yl-phosphonic acid
4
acid derivative
4
derivative grafted
4
grafted mesoporous
4
mesoporous silica
4
silica surface
4
surface novel
4
novel highly
4

Similar Publications

A strategically designed ternary nanohybrid (TNS-PDA/CNT), consisting of titanate nanosheet (TNS) and polydopamine-modified multiwalled carbon nanotube (PDA/CNT composite), was synthesized by the facile hydrothermal method and wet impregnation method for removal of U(VI) from aqueous solution and were characterized by transmission electron microscopy (TEM), scanning electron microscopy-energy-dispersive X-ray spectroscopy (SEM-EDS), X-ray diffraction (XRD), Fourier transform infrared (FT-IR), thermogravimetric analysis (TGA), Raman spectroscopy, Brunauer-Emmett-Teller (BET), and X-ray photoelectron spectroscopy (XPS). TNSs were introduced into the PDA/CNT composite, which effectively averted the agglomeration of the CNT and further exposed more adsorption sites. PDA thin layer exposing more active sites was conducive to enhance adsorption capacity and kinetic.

View Article and Find Full Text PDF

Flexible self-standing amidoxime-functionalized MXene membrane for electrochemical uranium extraction.

J Colloid Interface Sci

February 2025

Jiangxi Province Key Laboratory of Functional Organic Polymers, East China University of Technology, Nanchang 330013, Jiangxi, China. Electronic address:

The presence of radioactive U(VI) ions in sewage poses a significant threat to both the ecological environment and human health. In recent years, an electricity-driven remediation strategy has emerged as aprominent technique for the elimination of radionuclides. Specifically, the square wave transformation method is an emerging technology for electrochemical separation and enrichment of uranium.

View Article and Find Full Text PDF

Uranium extraction from seawater (UES) has important strategic significance for maintaining the sustainable development of nuclear energy. This article presents the preparation of a low-cost, efficient, and highly reusable biosorbent sodium alginate/polyethyleneimine (SA/PEI) through a simple one-step crosslinking process. The chemical crosslinking between PEI and SA provides biosorbent excellent mechanical strength and thermal stability.

View Article and Find Full Text PDF

The present work envisages a chelation driven, facile, selective, and rapid method for uranium(VI) separation from a (U, Th) mixture using 1-hydroxy-2-pyridone (1,2-HOPO). Herein, U(VI) was selectively precipitated as the neutral [UO(HOPO)(HO)]·HO (orange colored) complex while Th(IV) and other metal ions remained in the solution. The pH of the medium played a key role in facilitating the separation process.

View Article and Find Full Text PDF

Investigating the interaction of uranium(VI) with diatoms and their bacterial community: A microscopic and spectroscopic study.

Ecotoxicol Environ Saf

October 2024

SUBATECH, IMTA/CNRS-IN2P3/Université de Nantes, 4, rue Alfred Kastler, 44304 Nantes, France; LTSER "Zone Atelier Territoires Uranifères", Clermont-Ferrand, Aubière F-63000, France. Electronic address:

Diatoms and bacteria play a vital role in investigating the ecological effects of heavy metals in the environment. Despite separate studies on metal interactions with diatoms and bacteria, there is a significant gap in research regarding heavy metal interactions within a diatom-bacterium system, which closely mirrors natural conditions. In this study, we aim to address this gap by examining the interaction of uranium(VI) (U(VI)) with Achnanthidium saprophilum freshwater diatoms and their natural bacterial community, primarily consisting of four successfully isolated bacterial strains (Acidovorax facilis, Agrobacterium fabrum, Brevundimonas mediterranea, and Pseudomonas peli) from the diatom culture.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!