Abstract

Mercury emissions represent a significant risk to the environment and human health. Mercury is persistent and can circulate in the environment for thousands of years, which is why treating this toxic metal is important. Chitosan polymer is easily obtainable, and it has good mercury adsorption characteristics. This study aimed to improve its capabilities to absorb mercury by immobilizing phycobiliproteins (PBPs) onto the surface of chitosan beads (chitosan–PBPs). Phycobiliproteins, light-harvesting proteins from algae and cyanobacteria, have several industrially essential applications. These proteins can bind heavy metals with high affinities. Protein extracts obtained from both Arthrospira platensis, with C-phycocyanin (C-PC) as the primary protein, and Porphyra yezoensis, with R-phycocyanin (R-PC) and R-phycoerythrin (R-PE) as the dominant PBPs, were covalently immobilized onto chitosan beads. Beads with immobilized PBPs were characterized by scanning electron microscopy and Fourier transform infrared spectroscopy. Binding analysis showed that, on average, each chitosan bead weighed 20 mg and immobilized 63.54 μg of PBPs from Spirulina and 44.12 μg of PBPs from Porphyra. Immobilized proteins were still in their native state, with no visible color change months after immobilization. Chitosan–PBPs and chitosan alone were tested for mercury adsorption at pH 4 and pH 7 by atomic absorption spectroscopy. The tested concentration range of mercury was from 1 to 70 ppm. Affinity, calculated using Henry's binding isotherm, of chitosan–PBPs for mercury was twice as much higher at both pH values than chitosan alone. Furthermore, chitosan-PBP beads were able to absorb more mercury than chitosan alone. These results showed that the covalent immobilization of PBPs onto chitosan improves its mercury adsorption characteristics and creates a more efficient eco-friendly adsorbent to potentially remove mercury ions in the tested concentration range from polluted waters.

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