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Efficient removal of amine-modified polystyrene nanoplastics utilizing poly(N-isopropylacrylamide)-sodium carboxymethyl cellulose hydrogel beads: Parametric optimization and mechanistic insights

Authors
Mondal, SomenBaghel, KuldeepCho, SeongsuZahraLim, HosubLee, Jinkee
Issue Date
14-Aug-2025
Publisher
Elsevier B.V.
Keywords
Adsorption isotherms; Adsorption kinetics; Adsorption mechanism; Interpenetrating polymer network hydrogel; Polystyrene nanoplastics
Citation
Separation and Purification Technology, v.363
Indexed
SCIE
SCOPUS
Journal Title
Separation and Purification Technology
Volume
363
URI
https://scholarx.skku.edu/handle/2021.sw.skku/120856
DOI
10.1016/j.seppur.2025.132035
ISSN
1383-5866
1873-3794
Abstract
Nanoplastics (NPs), particularly positively charged NPs smaller than 100 nm, are emerging hazardous pollutants that pose a serious threat to aquatic ecosystems because of their non-biodegradable nature, ability to penetrate cell membranes, and tendency to form complexes. Therefore, the development of an effective adsorbent to remove positively charged nanosized NPs from contaminated water is crucial. In this study, interpenetrating polymer double-network (IPN) hydrogel beads composed of poly(N-isopropylacrylamide) (PNIPAM) and sodium carboxymethyl cellulose (NaCMC) were synthesized as adsorbents. The synthesis followed a photoinitiated free-radical mechanism in the presence of poly(ethylene glycol) diacrylate (PEGDA) as a cross-linking agent and 2-hydroxy-2-methylpropiophenone as a photoinitiator, utilizing a gas dynamic virtual nozzle (GDVN). For the first time, an IPN hydrogel synthesized by this approach was used to purify water containing positively charged amine-modified polystyrene (PS) NPs. Parametric optimization confirmed the effectiveness of the hydrogels for NPs elimination, achieving 99.83% removal efficiency (199.64 mg/g). The high efficiencies for the elimination of NPs from real seawater (99.55%) and tap water (98.11%), along with the sufficient adsorption capacity of 94.55% after five successive sorption/regeneration cycles, demonstrate the practical applicability of the synthesized hydrogel. The adsorption process followed a complex mechanism involving chemisorption/electrostatic bonding, as supported by the pseudo-second-order kinetics, Langmuir isotherms, and negative ΔG0 values, along with physical adsorption through H-bonding, π–π interactions, and pore filling. Considering its relatively high sorption capability, practical adaptability, and reusability, the synthesized IPN hydrogel is a viable option for treating NP-contaminated water. © 2025 Elsevier B.V.
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