TY - JOUR
T1 - Enhanced iodide removal from aqueous solutions using 3D-printed PLA scaffold coated with Cu/Cu2O nanoparticles
AU - Kim, Bokseong
AU - Park, Yuri
AU - Kim, Hyo Won
AU - Kim, Jin Ah
AU - Hwang, Yuhoon
N1 - Publisher Copyright:
© 2025 Elsevier Inc.
PY - 2025/8/15
Y1 - 2025/8/15
N2 - In nuclear power plant accidents, radioactive iodine (129I, 131I) can enter the environment, accumulate in the food chain, and pose significant health risks. We developed a novel scaffold using Cu/Cu2O nanoparticles immobilized on a polylactic acid 3D-printed scaffold for efficient iodide removal. The PLA scaffold was fabricated using a fused deposition modeling 3D printer, then surface-modified for enhanced hydrophilicity and functionalized with carboxyl groups via hydrolysis and acrylic acid grafting. Cu/Cu2O nanoparticles were immobilized on the modified surface. The adsorption capacity, determined using the Langmuir model, was 4.85 mg/g, and adsorption kinetics followed a pseudo-second-order model. The iodide removal mechanism was primarily driven by redox reactions between Cu(0), Cu(I) and iodide, leading to the formation of copper iodide (CuI), as confirmed by X-ray diffraction and Raman spectroscopy. Importantly, the Cu/Cu2O scaffold exhibited excellent structural stability during adsorption, with minimal copper leaching (<0.08 mg/L). Characterization of the Cu/Cu2O scaffold using scanning electron microscopy with energy-dispersive spectroscopy and X-ray photoelectron spectroscopy analysis supported these results. The scaffold demonstrated high selectivity for iodide ions even with competing anions. The scaffold maintained its effectiveness across a wide pH range, and continuous column tests separately confirmed its suitability for practical applications in environmental remediation and wastewater treatment systems. In summary, we successfully fabricated a 3D-printed Cu/Cu2O-PLA scaffold, demonstrated its efficient iodide removal performance, and elucidated the underlying redox-driven adsorption mechanism.
AB - In nuclear power plant accidents, radioactive iodine (129I, 131I) can enter the environment, accumulate in the food chain, and pose significant health risks. We developed a novel scaffold using Cu/Cu2O nanoparticles immobilized on a polylactic acid 3D-printed scaffold for efficient iodide removal. The PLA scaffold was fabricated using a fused deposition modeling 3D printer, then surface-modified for enhanced hydrophilicity and functionalized with carboxyl groups via hydrolysis and acrylic acid grafting. Cu/Cu2O nanoparticles were immobilized on the modified surface. The adsorption capacity, determined using the Langmuir model, was 4.85 mg/g, and adsorption kinetics followed a pseudo-second-order model. The iodide removal mechanism was primarily driven by redox reactions between Cu(0), Cu(I) and iodide, leading to the formation of copper iodide (CuI), as confirmed by X-ray diffraction and Raman spectroscopy. Importantly, the Cu/Cu2O scaffold exhibited excellent structural stability during adsorption, with minimal copper leaching (<0.08 mg/L). Characterization of the Cu/Cu2O scaffold using scanning electron microscopy with energy-dispersive spectroscopy and X-ray photoelectron spectroscopy analysis supported these results. The scaffold demonstrated high selectivity for iodide ions even with competing anions. The scaffold maintained its effectiveness across a wide pH range, and continuous column tests separately confirmed its suitability for practical applications in environmental remediation and wastewater treatment systems. In summary, we successfully fabricated a 3D-printed Cu/Cu2O-PLA scaffold, demonstrated its efficient iodide removal performance, and elucidated the underlying redox-driven adsorption mechanism.
KW - 3D printing technology
KW - Adsorption mechanism
KW - Copper oxide nanoparticles
KW - Filter-type adsorbent
KW - Radioactive iodine
UR - https://www.scopus.com/pages/publications/105005253203
U2 - 10.1016/j.envres.2025.121835
DO - 10.1016/j.envres.2025.121835
M3 - Article
C2 - 40378996
AN - SCOPUS:105005253203
SN - 0013-9351
VL - 279
JO - Environmental Research
JF - Environmental Research
M1 - 121835
ER -