Evidence map›Paper›PMID 36678117›Full record

ReviewNanomaterials (Basel, Switzerland)2023

Uranium Removal from Aqueous Solutions by Aerogel-Based Adsorbents-A Critical Review.

Efthalia Georgiou, Grigorios Raptopoulos, Ioannis Anastopoulos, Dimitrios A Giannakoudakis, Michael Arkas, Patrina Paraskevopoulou, Ioannis Pashalidis

Abstract readReview
In one paragraph

Review in Nanomaterials (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Nanoscale Materials for Water Purification and Catalysis.Nanomaterials (Basel, Switzerland) · 2025
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Removal ofMolecules (Basel, Switzerland) · 2023
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Efthalia GeorgiouRadioanalytical and Environmental Chemistry Group, Department of Chemistry, University of Cyprus, P.O. Box 20537, Nicosia CY-1678, Cyprus.
Grigorios RaptopoulosInorganic Chemistry Laboratory, Department of Chemistry, National and Kapodistrian University of Athens, Panepistimiopolis Zografou, 15771 Athens, Greece.ORCID 0000-0001-9763-2431
Ioannis AnastopoulosDepartment of Agriculture, University of Ioannina, UoI Kostakii Campus, 47100 Arta, Greece.ORCID 0000-0002-3371-3731
Dimitrios A GiannakoudakisDepartment Chemistry, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece.ORCID 0000-0001-5996-6510
Michael ArkasDemokritos National Centre for Scientific Research, Institute of Nanoscience and Nanotechnology, 15771 Athens, Greece.ORCID 0000-0001-8881-3361
Patrina ParaskevopoulouInorganic Chemistry Laboratory, Department of Chemistry, National and Kapodistrian University of Athens, Panepistimiopolis Zografou, 15771 Athens, Greece.ORCID 0000-0002-5166-8946
Ioannis PashalidisRadioanalytical and Environmental Chemistry Group, Department of Chemistry, University of Cyprus, P.O. Box 20537, Nicosia CY-1678, Cyprus.ORCID 0000-0002-7587-6395

Funding

European Cooperation in Science and Technology CA18125
6 · The paper itself

Abstract

Aerogels are a class of lightweight, nanoporous, and nanostructured materials with diverse chemical compositions and a huge potential for applications in a broad spectrum of fields. This has led the IUPAC to include them in the top ten emerging technologies in chemistry for 2022. This review provides an overview of aerogel-based adsorbents that have been used for the removal and recovery of uranium from aqueous environments, as well as an insight into the physicochemical parameters affecting the adsorption efficiency and mechanism. Uranium removal is of particular interest regarding uranium analysis and recovery, to cover the present and future uranium needs for nuclear power energy production. Among the methods used, such as ion exchange, precipitation, and solvent extraction, adsorption-based technologies are very attractive due to their easy and low-cost implementation, as well as the wide spectrum of adsorbents available. Aerogel-based adsorbents present an extraordinary sorption capacity for hexavalent uranium that can be as high as 8.8 mol kg−1 (2088 g kg−1). The adsorption data generally follow the Langmuir isotherm model, and the kinetic data are in most cases better described by the pseudo-second-order kinetic model. An evaluation of the thermodynamic data reveals that the adsorption is generally an endothermic, entropy-driven process (ΔH0, ΔS0 > 0). Spectroscopic studies (e.g., FTIR and XPS) indicate that the adsorption is based on the formation of inner-sphere complexes between surface active moieties and the uranyl cation. Regeneration and uranium recovery by acidification and complexation using carbonate or chelating ligands (e.g., EDTA) have been found to be successful. The application of aerogel-based adsorbents to uranium removal from industrial processes and uranium-contaminated waste waters was also successful, assuming that these materials could be very attractive as adsorbents in water treatment and uranium recovery technologies. However, the selectivity of the studied materials towards hexavalent uranium is limited, suggesting further developments of aerogel materials that could be modified by surface derivatization with chelating agents (e.g., salophen and iminodiacetate) presenting high selectivity for uranyl moieties.

Indexed as

adsorption thermodynamics and kineticsaerogelscompetitive ionsenvironmental remediationenvironmental water decontaminationextraordinary adsorption capacitymaterial recyclingqmax valuesuranium adsorptionuranium recovery

Identifiers

PMID36678117
PMCPMC9866664

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.