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Mechanistic investigation on the green recovery of ionic, nanocrystalline, and metallic gold by two anionic nanocelluloses

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Title
Mechanistic investigation on the green recovery of ionic, nanocrystalline, and metallic gold by two anionic nanocelluloses
Author
Dwivedi, Amarendra DharDubey, Shashi PrabhaHokkanen, SannaSillanpaa, Mika
Issue Date
2014-10
Publisher
ELSEVIER SCIENCE SA
Citation
CHEMICAL ENGINEERING JOURNAL, v.253, pp.316 - 324
Abstract
The modified cellulose (ADAC samples) used as backbone to obtain biodegradable hydrogels, which demonstrated high affinity to concentrate precious gold species. The primary foci of the study were to develop green techniques to recover Au from dilute solutions by providing the mechanistic evidences for the adsorption coupled reduction pathways. The derivatives of anionic nanocellulose were used for recovery of the ionic, nanoparticulate, and metallic forms of Au. The ADAC samples were promising sorbing phase (57 and 60. mg/g capacity) even at low pH for the treatment of the gold-polluted waters. Thermodynamically, ADAC hydrogels were remained active at moderate to higher temperature (295-333. K) in an endothermic way. Reduction of Au occurred at different stages of kinetic curves, facilitating the formation of zerovalent gold (48 and 41. nm particle size). The Au recovery minimally altered by the competing heavy metals (Cd, Co, Cr, Ni, and As), either at equivalent or lower concentrations. A significant amount of Au(III) (83-99%) regenerated by a strong complexing eluent (0.5. M thiourea in 1. M HCl), moreover thermal crystallization yielded metallic gold in an excellent amount (94%). The mechanism of adsorptive-reduction of gold-nanocellulose were investigated and characterized by the spectroscopic studies including X-ray photoelectron spectroscopy. Overall, recovery of gold in desired forms from nanocellulose can be viewed as an effective biomaterial management strategy.
URI
https://scholarworks.unist.ac.kr/handle/201301/5085
URL
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84902012191
DOI
10.1016/j.cej.2014.05.069
ISSN
1385-8947
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