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Adsorption in a Fixed-Bed Column and Stability of the Antibiotic Oxytetracycline Supported on Zn(II)-[2-Methylimidazolate] Frameworks in Aqueous Media
Author(s) -
Janine dos Santos Ferreira da Silva,
Daniel López-Malo,
Giovana A. Bataglion,
Marcos N. Eberlin,
Célia M. Ronconi,
Severino Alves Júnior,
Gilberto F. de Sá
Publication year - 2015
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0128436
Subject(s) - adsorption , oxytetracycline , scanning electron microscope , zinc , nuclear chemistry , aqueous solution , elution , chemistry , infrared spectroscopy , metal , chromatography , materials science , antibiotics , organic chemistry , biochemistry , composite material
A metal-organic framework, Zn-[2-methylimidazolate] frameworks (ZIF-8), was used as adsorbent material to remove different concentrations of oxytetracycline (OTC) antibiotic in a fixed-bed column. The OTC was studied at concentrations of 10, 25 and 40 mg L -1 . At 40 mg L -1 , the breakthrough point was reached after approximately 10 minutes, while at 10 and 25 mg L -1 this point was reached in about 30 minutes. The highest removal rate of 60% for the 10 mg L -1 concentration was reached after 200 minutes. The highest adsorption capacity (28.3 mg g -1 ) was attained for 25 mg L -1 of OTC. After the adsorption process, a band shift was observed in the UV-Vis spectrum of the eluate. Additional studies were carried out to determine the cause of this band shift, involving a mass spectrometry (MS) analysis of the supernatant liquid during the process. This investigation revealed that the main route of adsorption consisted of the coordination of OTC with the metallic zinc centers of ZIF-8. The materials were characterized by thermal analysis (TA), scanning electron microscopy (SEM), powder X-ray diffraction (XRD), and infrared spectroscopy (IR) before and after adsorption, confirming the presence of OTC in the ZIF-8 and the latter’s structural stability after the adsorption process.

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