“…This trend showed a linear increase up to a maximum value at 2375 mg g À1 within an adsorption time of 1 h and then slightly decreased at the initial concentration above 1200 mg L À1 . The superior maximum adsorption value of 2375 mg g À1 towards CR adsorption in solution at various initial concentrations in the range of 400-1400 mg L À1 for 1 h at natural pH and room temperature on the as-obtained MgO adsorbent was nearly equal to the reported superhigh adsorption capacity, 1,30 which was superior to that in most reports. 16,25,28,37 This showed that MgO nanoparticles prepared via the facile solvent-free chemical reaction manifested outstanding adsorption properties.…”
Section: Characterization Of Mgo Nanoparticlesmentioning
confidence: 63%
“…1c shows TEM and HRTEM images of the MgO nanoparticles with average particle diameters of approximately 10 nm, indicating a distinct lattice space of 0.21 nm, which corresponded well with the normal (200) plane, and was consistent with reported data. 30 MgO nanoparticles with an average diameter of about 10 nm had been successfully prepared by a facile solvent-free strategy using the reaction between Mg(OAc) 2 and H 2 C 2 O 4 . Compared with the particles size of MgO prepared using other synthetic methods in previous reports, the obtained MgO nanoparticles were much smaller, probably owing to the different microenvironment of the directcontact solid-state chemical reaction relative to solution synthesis.…”
Section: Characterization Of Mgo Nanoparticlesmentioning
confidence: 99%
“…29 Lamellar MgO nanostructures with alkaline surfaces have been successfully synthesized via hydrothermal synthesis, and demonstrated a superior adsorption performance towards Congo red solutions with an adsorption capacity of 2650 mg g À1 . 30 Other MgO nanomaterials with different morphologies have also been synthesized in solution. [25][26][27][28][29] However, their synthesis usually requires complex preparation processes owing to multistep synthetic operations under solution conditions, resulting in unnecessary environmental pollution from the organic agents.…”
“…This trend showed a linear increase up to a maximum value at 2375 mg g À1 within an adsorption time of 1 h and then slightly decreased at the initial concentration above 1200 mg L À1 . The superior maximum adsorption value of 2375 mg g À1 towards CR adsorption in solution at various initial concentrations in the range of 400-1400 mg L À1 for 1 h at natural pH and room temperature on the as-obtained MgO adsorbent was nearly equal to the reported superhigh adsorption capacity, 1,30 which was superior to that in most reports. 16,25,28,37 This showed that MgO nanoparticles prepared via the facile solvent-free chemical reaction manifested outstanding adsorption properties.…”
Section: Characterization Of Mgo Nanoparticlesmentioning
confidence: 63%
“…1c shows TEM and HRTEM images of the MgO nanoparticles with average particle diameters of approximately 10 nm, indicating a distinct lattice space of 0.21 nm, which corresponded well with the normal (200) plane, and was consistent with reported data. 30 MgO nanoparticles with an average diameter of about 10 nm had been successfully prepared by a facile solvent-free strategy using the reaction between Mg(OAc) 2 and H 2 C 2 O 4 . Compared with the particles size of MgO prepared using other synthetic methods in previous reports, the obtained MgO nanoparticles were much smaller, probably owing to the different microenvironment of the directcontact solid-state chemical reaction relative to solution synthesis.…”
Section: Characterization Of Mgo Nanoparticlesmentioning
confidence: 99%
“…29 Lamellar MgO nanostructures with alkaline surfaces have been successfully synthesized via hydrothermal synthesis, and demonstrated a superior adsorption performance towards Congo red solutions with an adsorption capacity of 2650 mg g À1 . 30 Other MgO nanomaterials with different morphologies have also been synthesized in solution. [25][26][27][28][29] However, their synthesis usually requires complex preparation processes owing to multistep synthetic operations under solution conditions, resulting in unnecessary environmental pollution from the organic agents.…”
“…Liu et al [14] aimed a study on Mg(OH)2 as an adsorbent for methyl orange. Then the study by Liu et al [15] showed that the adsorption of congo red on Mg(OH)2 and MgO occurs through surface exchange until the surface function sites are fully occupied. The dye molecules are diffused for further adsorption reactions (complexation interactions).…”
The study of Mg(OH)2 from seawater bittern as an adsorbent for Congo red (CR) from an aqueous solution has been performed. This study aimed to determine the effect of pH, contact time, and initial CR concentration on CR adsorption by Mg(OH)2. The adsorption kinetics and isotherms of CR on Mg(OH)2 in an aqueous solution were also studied. The optimum adsorption was obtained at pH 8 within 90 minutes of contact time with an adsorption capacity of 46.3 mg/g for an initial CR concentration of 29 mg/L. The adsorption process followed the Freundlich isotherm model with an n value of 2.579 and the pseudo-second-order kinetic model with a k2 value of 0.0021 g mg−1min−1.
“…The maximum adsorption capacity of lamellar MgO can reach up to 2650 mg g À1 . 36 In despite of these achievements at present, the synthesis methods and the adsorption capacities of MgO need to be further improved.…”
Porous MgO-hex and MgO-dhp materials were synthesized by annealing metal–organic framework [NH4][Mg(HCOO)3], and exhibit excellent adsorption capacities toward Congo red.
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