Please use this identifier to cite or link to this item: https://idr.l2.nitk.ac.in/jspui/handle/123456789/12887
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dc.contributor.authorRaja, C.P.-
dc.contributor.authorJacob, J.M.-
dc.contributor.authorRaj Mohan, Balakrishnan-
dc.date.accessioned2020-03-31T08:42:21Z-
dc.date.available2020-03-31T08:42:21Z-
dc.date.issued2016-
dc.identifier.citationJournal of Environmental Engineering (United States), 2016, Vol.142, 9, pp.-en_US
dc.identifier.urihttps://idr.nitk.ac.in/jspui/handle/123456789/12887-
dc.description.abstractExperiments were conducted to study the Selenium (Se) biosorption and recovery by marine Aspergillus terreus in an upflow bioreactor for a period of 8 days. The Se tolerance of the marine fungus was initially confirmed by visual and microscopic observations that evinced intact fungal cells in an Se-amended medium with sparse changes in the spore texture and cellular number by the seventh day of biosorption studies in the upflow bioreactor. Further, the effect of pH and contact time on the percentage of Se biosorption, in an upflow bioreactor containing fungal pellets, was investigated. It was analyzed that pH ranges of 6-7 and a contact time of 5 days resulted in 85-87% biosorption of Se by the fungal biomass. The interaction of the fungus with the induced Se stress in the medium was monitored regularly for studying the uptake of the metalloid and the possible biosynthesis of Se nanoparticles. Analyses using ultraviolet visible (UV-Vis) spectroscopy, scanning electron microscopy (SEM), and X-ray diffraction (XRD) studies revealed the formation of crystalline Se nanocrystals with an average diameter of 500 nm on the fungal cell wall. Fourier transform infrared (FTIR) spectroscopic analysis indicated the possible involvement of fungal protein groups that aid the binding of the biosorbed Se nanoparticles on to the fungal cell wall. 2015 American Society of Civil Engineers.en_US
dc.titleSelenium Biosorption and Recovery by Marine Aspergillus terreus in an Upflow Bioreactoren_US
dc.typeArticleen_US
Appears in Collections:1. Journal Articles

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