Source abstract
Abstract
In this paper, the potential use of either amine-functionalized or hydroxyl-functionalized magnesium ferrite (MgFe2O4) nanoparticles (NPs) as Congo red nanoadsorbents is explored and compared. The amine-functionalized MgFe2O4 NPs (denoted as MgFe2O4–NH2 NPs) were synthesized by a one-pot coprecipitation method using ethanolamine as a surface modifier, while the hydroxyl-functionalized MgFe2O4 NPs (denoted as MgFe2O4–OH NPs) were prepared by a hydrothermal method. In general, both nanoadsorbents can be successfully produced without calcination and were found to possess superparamagnetic properties with high saturation magnetization (Ms). In particular, MgFe2O4–OH NPs exhibit a higher Ms value of ∼53 emu g–1, promoting the rapid separation ability of the NPs from the treated solution using an external permanent magnet. The Congo red removal performance of these nanoadsorbents was investigated as a function of the pH of the aqueous solution and contact time. The removal efficiency of Congo red by MgFe2O4–NH2 NPs was found to be ∼96% within 180 min at pH 6, while MgFe2O4–OH NPs provided a removal efficiency at ∼88% within 420 min at pH 8. In addition, the maximum adsorption capacities (qm) calculated using the Langmuir isotherm equation were found to be 71.4 and 67.6 mg g–1 for MgFe2O4–NH2 and MgFe2O4–OH NPs, respectively. The higher qm value of MgFe2O4–NH2 NPs could be attributed to stronger electrostatic interactions with the sulfonate groups of Congo red formed by larger numbers of protonated amine groups than protonated hydroxyl groups of the adsorbents under the performed conditions. Moreover, reusability experiments also revealed that MgFe2O4–NH2 NPs offered a higher removal efficiency than MgFe2O4–OH NPs for the same cycles tested. Therefore, this study demonstrates that MgFe2O4–NH2 NPs synthesized by a simple one-pot synthetic method are applicable as reusable magnetic nanoadsorbents for Congo red removal in current practice.
Source: openalex_inverted_index · Quality: baseline
Affiliations
Department of Chemistry and Center of Excellence for Innovation in Chemistry, Faculty of Science, Chiang Mai University, Chiang Mai 50200, Thailand
Graduate School, Chiang Mai University, Chiang Mai 50200, Thailand
Advanced Materials Physics Laboratory (Amp.), School of Physics, Institute of Science, Suranaree University of Technology, Nakhon Ratchasima 30000, Thailand
Laboratory of Cell-Based Assays and Innovations, School of Biotechnology, Institute of Agricultural Technology, Suranaree University of Technology, 111 University Avenue, Nakhon Ratchasima 30000, Thailand
Institute of Nanomaterials Research and Innovation for Energy (IN-RIE), Khon Kaen University, Khon Kaen 40002, Thailand
Department of Physics and Materials Science, Faculty of Science, Chiang Mai University, Chiang Mai 50200, Thailand
Center of Excellence in Materials Science and Technology, Chiang Mai University, Chiang Mai 50200, Thailand