TY - JOUR
T1 - Functionalized 3D polyurethane foams with microwave-synthesized TiO2 nanostructures for solar light-driven degradation of tetracycline
AU - Matias, Maria Leonor
AU - Pimentel, Ana
AU - Reis Machado, Ana S.
AU - Rodrigues, Joana
AU - Fernandes, Auguste
AU - Monteiro, Teresa
AU - Almeida Carvalho, Patrícia
AU - Amaral, Mariana N.
AU - Reis, Catarina Pinto
AU - Deuermeier, Jonas
AU - Fortunato, Elvira
AU - Martins, Rodrigo
AU - Nunes, Daniela
N1 - Publisher Copyright:
© 2025 RSC.
PY - 2025/1/23
Y1 - 2025/1/23
N2 - Pharmaceutical substances present in soils and water supplies pose a significant risk to the ecosystem. Solar light-driven photocatalysis with titanium dioxide (TiO2) nanophotocatalysts has been widely explored for the degradation of these substances in aquatic resources. However, the lack of reported sustainable methods to produce TiO2 nanophotocatalysts and the challenges associated with their use in powder form during photocatalytic experiments further limit their scale-up. Herein, we show an eco-friendly approach to synthesize TiO2 nanopowders using a fast microwave method (10 min) and their further incorporation on polyurethane (PU) foams by a simple dip-coating process. Ethanol, isopropanol (IPA), and water were employed for the microwave synthesis of TiO2 nanophotocatalysts, unveiling distinct structural and optical properties for the material synthesized in each solvent. When ethanol was used as a solvent, TiO2 anatase nanocrystals were obtained, which exhibited high-index {012}/{102} facets with surface steps and bulk defects. These defects together with the superior specific surface area and higher capacity for surface oxygen adsorption contributed to a significant adsorption capacity (about 58% in 240 min) of tetracycline (TC) and overall TC removal of ∼90% after 30 min of simulated solar light exposure. Reusable TiO2-PU foams achieved ∼80% of TC removal in 180 min of light exposure. This study showcases the successful surface modification of PU foams with TiO2 nanostructures highlighting their potential for an efficient removal of tetracycline from water while ensuring ecological safety, as demonstrated by the ecotoxicity assays using the Artemia salina model.
AB - Pharmaceutical substances present in soils and water supplies pose a significant risk to the ecosystem. Solar light-driven photocatalysis with titanium dioxide (TiO2) nanophotocatalysts has been widely explored for the degradation of these substances in aquatic resources. However, the lack of reported sustainable methods to produce TiO2 nanophotocatalysts and the challenges associated with their use in powder form during photocatalytic experiments further limit their scale-up. Herein, we show an eco-friendly approach to synthesize TiO2 nanopowders using a fast microwave method (10 min) and their further incorporation on polyurethane (PU) foams by a simple dip-coating process. Ethanol, isopropanol (IPA), and water were employed for the microwave synthesis of TiO2 nanophotocatalysts, unveiling distinct structural and optical properties for the material synthesized in each solvent. When ethanol was used as a solvent, TiO2 anatase nanocrystals were obtained, which exhibited high-index {012}/{102} facets with surface steps and bulk defects. These defects together with the superior specific surface area and higher capacity for surface oxygen adsorption contributed to a significant adsorption capacity (about 58% in 240 min) of tetracycline (TC) and overall TC removal of ∼90% after 30 min of simulated solar light exposure. Reusable TiO2-PU foams achieved ∼80% of TC removal in 180 min of light exposure. This study showcases the successful surface modification of PU foams with TiO2 nanostructures highlighting their potential for an efficient removal of tetracycline from water while ensuring ecological safety, as demonstrated by the ecotoxicity assays using the Artemia salina model.
UR - http://www.scopus.com/inward/record.url?scp=105003922582&partnerID=8YFLogxK
U2 - 10.1039/d4va00110a
DO - 10.1039/d4va00110a
M3 - Article
AN - SCOPUS:105003922582
SN - 2754-7000
VL - 4
SP - 713
EP - 738
JO - Environmental Science: Advances
JF - Environmental Science: Advances
IS - 5
ER -