Application of a novel polymer cross-linked with magnetite for efficient norfloxacin adsorption at a wide pH range.

Nowadays, NOR-containing wastewater has placed huge pressure on global ecology. In this study, a chemically-modified chitosan-based polymer was cross-linked with magnetite to prepare a novel magnetic composite adsorbent named Fe3O4/CS-P(AM-SSS) for norfloxacin (NOR) removal. The preparation conditions were optimized by single factor experiments and response surface methodology. A series of characterization analyses were carried out on the morphology, structure, and properties of Fe3O4/CS-P(AM-SSS), verifying that Fe3O4/CS-P(AM-SSS) was successfully prepared. Batch adsorption experiments showed that NOR was efficiently removed by Fe3O4/CS-P(AM-SSS), with a broad pH applicability of 3-10, short adsorption equilibrium time of 60 min, maximum adsorption capacity of 268.79 mg/g, and high regeneration rate of 86% after eight adsorption-desorption cycles. Due to the three-dimensional network structure and abundant functional groups provided by modified chitosan polymer, the superior adsorption capability of Fe3O4/CS-P(AM-SSS) was achieved through electrostatic interaction, π-π stacking, hydrophobic interaction, and hydrogen bonding. Adsorption process was exothermic and well fitted by the pseudo-second-order kinetic model and the Langmuir isothermal model. The presence of cations had a slight inhibitory effect on NOR adsorption, while humic acid nearly had no effect. In model swine wastewater, 90.3% NOR was removed by Fe3O4/CS-P(AM-SSS). Therefore, with these superior characteristics, Fe3O4/CS-P(AM-SSS) was expected to be an ideal material for treating NOR-containing wastewater in the future.

Photocatalytic activity evaluation of polyvinylpyrrolidone K30 assisted synthesis of 1D oxygen-vacancy-rich Bi5O7BrxI1-x nanorod solid solution.

The unique layered structure of bismuth halide oxide has led to an extensive application in the degradation of refractory antibiotics from water environments. With the aid of regulating the energy band structure of photocatalytic materials and equilibrating the response towards visible light and redox ability, a novel oxygen-vacancy-rich Bi5O7BrxI1-x nanorod solid solution was synthesized by polyvinylpyrrolidone K30 assisted solvothermal method, and its photocatalytic behavior was investigated for the degradation of antibiotic levofloxacin under visible light. The degradation rate of the optimal Bi5O7Br0.5I0.5 to levofloxacin can reach 82.7% within 30 min, which is 9.22 and 4.74 times higher than those of the monomers Bi5O7Br and Bi5O7I. The catalyst of Bi5O7Br0.5I0.5 shows 99.88% antibacterial activity against Escherichia coli. The efficient photocatalytic ability of the Bi5O7Br0.5I0.5 is resulted from the alteration of energy band structure and suppression of charge recombination due to benign changes in the electronic and crystal structures. Furthermore, both various characterizations and Density Functional Theory calculations reveal that a multitude of oxygen vacancies exist in the Bi5O7Br0.5I0.5. The photocatalytic degradation pathways were explored and the toxicity of the intermediates was also appraised. The present work provides a mild and feasible construction of solid solutions and introduction of oxygen vacancies to eliminate environmentally refractory organic pollutants with photocatalytic technology.