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- W2970073160 abstract "Doxorubicin (DOX) originated from users’ urine has been an emerging environmental pollutant due to its significant genotoxicity to mankind. Thus, urine source separation is a potential strategy to isolate DOX at a higher concentration and reduce the burden of downstream wastewater treatment. To develop highly efficient, easy separation and retrievable materials for individual patient to conveniently remove DOX from own urine, magnetic Cu3(PO4)2 nanoflowers were prepared through anchoring amino-functionalized magnetic nanoparticles on the Cu3(PO4)2 nanoflowers. Characterizations revealed the magnetic nanoflowers were spherical in shape with a mean size of 15 μm, and porous and hierarchical in structure. Magnetic nanoparticles located the surface of petals. Multibatch experiments were performed to assess the removal performance of DOX from aqueous solution. The magnetic nanoflowers exhibited excellent removal efficiency of DOX under weakly alkaline condition at ambient temperature. Linear and non-linear analyses were carried out to compare the best fitting kinetics and isotherms. Sorption kinetic data best fitted the pseudo-second order model. The Freundlich isotherm explained equilibrium sorption data with R2 = 0.993 higher than that for the Langmuir isotherm. When the pH of synthetic urine was adjusted to weakly alkaline (pH 8.0–9.0), over 95% of DOX (20 mg L−1) was removed by a little of magnetic nanoflowers (50 mg L−1) within 5 min. Meanwhile, the magnetic nanoflowers could be easily separated and recovered from the synthetic urine by a magnet. So, for individual urine source separation strategy, the magnetic nanoflower seems to be an efficient, convenient and inexpensive approach to remove DOX from human urine." @default.
- W2970073160 created "2019-09-05" @default.
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- W2970073160 date "2020-01-01" @default.
- W2970073160 modified "2023-10-14" @default.
- W2970073160 title "Removal of doxorubicin by magnetic copper phosphate nanoflowers for individual urine source separation" @default.
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- W2970073160 doi "https://doi.org/10.1016/j.chemosphere.2019.124690" @default.
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