| Literature DB >> 34341658 |
Ackmez Mudhoo1, Mika Sillanpää2,3.
Abstract
Pure water will become a golden resource in the context of the rising pollution, climate change and the recycling economy, calling for advanced purification methods such as the use of nanostructured adsorbents. However, coming up with an ideal nanoadsorbent for micropollutant removal is a real challenge because nanoadsorbents, which demonstrate very good performances at laboratory scale, do not necessarily have suitable properties in in full-scale water purification and wastewater treatment systems. Here, magnetic nanoadsorbents appear promising because they can be easily separated from the slurry phase into a denser sludge phase by applying a magnetic field. Yet, there are only few examples of large-scale use of magnetic adsorbents for water purification and wastewater treatment. Here, we review magnetic nanoadsorbents for the removal of micropollutants, and we explain the integration of magnetic separation in the existing treatment plants. We found that the use of magnetic nanoadsorbents is an effective option in water treatment, but lacks maturity in full-scale water treatment facilities. The concentrations of magnetic nanoadsorbents in final effluents can be controlled by using magnetic separation, thus minimizing the ecotoxicicological impact. Academia and the water industry should better collaborate to integrate magnetic separation in full-scale water purification and wastewater treatment plants.Entities:
Keywords: Magnetic nanoadsorbents; Magnetic separation; Wastewater treatment; Water purification
Year: 2021 PMID: 34341658 PMCID: PMC8320315 DOI: 10.1007/s10311-021-01289-6
Source DB: PubMed Journal: Environ Chem Lett ISSN: 1610-3653 Impact factor: 9.027
Fig. 1Conceptual representation of the use of magnetic nanoadsorbents and integration of magnetic separation in existing wastewater treatment facilities for micropollutant removal. This concept is envisioned in three major phases. First, the effluent from the secondary treatment stage is treated with selected magnetic nanoadsorbent. This phase will be an advanced treatment. Second, the treated effluent from the advanced treatment phase is processed in an integrated magnetic separation system, where the micropollutant-laden magnetic nanoadsorbents are decoupled from the purified wastewater. Third, the purified water and micropollutant-loaded magnetic nanoadsorbents are separated in two different streams for further use and processing. The micropollutant-loaded magnetic nanoadsorbents are then regenerated. Created with BioRender.com.
Highlights of laboratory-scale adsorption performance of selected magnetic nanoadsorbents for micropollutants
| Adsorbent | Micropollutant | Highlights of adsorption behavior | References |
|---|---|---|---|
| Magnetic CrFe2O4 nanocomposite prepared sonochemically using a nonionic surfactant | Mo6+ | Thermodynamic data indicated that adsorption of Mo6+ ions was spontaneous and endothermic | Gamal et al. ( |
| The adsorbent could be regenerated through the desorption of more than 98% of Mo6+ with 1.0 mol L−1 sodium hydroxide | |||
| Magnetic nanocomposite Co-multiwalled carbon nanotubes | Methylene blue | Maximum adsorption capacity=324.34 mg g−1 | Çalımlı ( |
| Adsorption was endothermic and followed pseudo-second-order kinetic model | |||
| Fe3O4-MnO2-EDTA composite | Cu2+ ions from binary or ternary metal adsorbate system | As-synthesized adsorbents yielded high Cu2+ selective adsorption (both in binary and ternary systems) | Chen and Xie ( |
| In comparison with Fe3O4-MnO2, the magnetic Fe3O4-MnO2-EDTA nanoparticles resulted in rapid magnetic separation with high selectivity for Cu2+ | |||
| Magnetic CoFe2O4/graphene oxide adsorbents | Methylene blue, methyl orange and Rhodamine B | Adsorption of organic dyes for CoFe2O4/graphene oxide composite mainly attributable to contribution of graphene oxide | Chang et al. ( |
| Superior adsorption capacity | |||
| Selective adsorption with order of adsorption capacity as follows: Methylene blue > Rhodamine B > methyl orange | |||
| Hydroxypropyl-β- cyclodextrin-polyurethane/graphene oxide magnetic nanoconjugates | Cr6+ and Pb2+ | Adsorption capacity of adsorbents for Cr6+ and Pb2+ at 987 mg g−1 and 1399 mg g−1, respectively, and adsorption followed pseudo-second-order kinetics | Nasiri and Alizadeh ( |
| Reusability of adsorbent makes it a promising candidate for Pb2+ removal from aqueous solutions | |||
| This magnetic composite was endowed with a high adsorption performance and good reusability for heavy metal ions | |||
| Magnetic molecular imprint polymer networks synthesized from vinyl-functionalized magnetic nanoparticles | Antibiotics (ciprofloxacin and erythromycin) | Networks exhibited high binding capacity toward erythromycin and ciprofloxacin at 70 mg g−1 and 32 mg g−1, respectively. | Kuhn et al. ( |
| Networks were recyclable and retained their binding capacity after 4 cycles | |||
| Results demonstrated that the networks developed had high binding capacity, selectivity and recyclability | |||
| The networks can be utilized both for monitoring and removal of hazardous antibiotic pollutants potentially present in different samples and food products | |||
| Phosphoramide-functionalized magnetic nanoparticles | Uranium | High maximum adsorption capacity=95.2 mg U g−1 sorbent | Singhal et al. ( |
| 80% adsorption achieved for pH 4–8 with maximum adsorption observed at pH 6 | |||
| Higher than 90% uranium extraction was recorded during adsorption studies conducted using drinking water, tap water and seawater | |||
| Inferences were made in the study as follows: high adsorption capacity, low cost, less equilibration time, easy separation from matrix and non-toxicity of the adsorbent constitute some key merits sought when envisioning the process at an industrial scale | |||
| Magnetic tubular carbon nanofibers | Cu2+ | Maximum adsorption capacity of nanofibers for Cu2+=375.93 mg g−1 | Ahmad et al. ( |
| Porous morphology, large surface area and tubular structure of the nanofibers contributed to the rapid and highest adsorption of Cu2+ ions | |||
| Langmuir adsorption isotherm model best described adsorption data | |||
| The nanofibers developed have exhibited excellent regenerability when treated with EDTA | |||
| Magnesium–zinc ferrites | Cr6+ and Ni2+ | Mg0·2Zn0·8Fe2O4 yielded best adsorption capacity (30.49 mg g−1) | Tatarchuk et al. ( |
| Mg0·4Zn0·6Fe2O4 was observed to be the most effective adsorbent for removing Ni2+ (93.2%) | |||
| Adjustment of magnesium content to an optimal value can enhance mixed ferrites’ ability to remove heavy metals from aqueous solutions | |||
| Sulfur-functionalized polyamidoamine dendrimer/magnetic Fe3O4 hybrid materials | Hg2+ and Ag+ | Maximum adsorption capacity for Hg2+ and Ag+ was 0.8 mmol g−1 and 1.29 mmol g−1, respectively | Luan et al. ( |
| Good adsorption selectivity (100% selective adsorption of Hg2+ in the presence of Ni2+, Zn2+ and Mn2+) | |||
| Excellent regeneration characteristics, and reuse repeatedly over four use cycles | |||
| Magnetic sodium alginate (SA)-based Fe3O4@SA-Ca gel beads | Direct Orange 26 in aqueous solutions | Gel had ultrahigh adsorption capacity of 1252 mg g−1 | Li and Lin ( |
| Dye removal efficiency=96.2 % (298 K, 50 mg polymer dosage, 2.6 g L−1 initial dye concentration, pH 2.0, 90 min adsorption time) | |||
| Adsorption was spontaneous and exothermic | |||
| Gel was easily separated and recuperated from aqueous solutions without secondary pollution |
EDTA Ethylenediaminetetraacetic acid, SA Sodium alginate