Please use this identifier to cite or link to this item: https://doi.org/10.1002/jctb.280590106
DC FieldValue
dc.titleRecovery of gold by electroless precipitation from acid solutions using polyaniline
dc.contributor.authorTing, Y.P.
dc.contributor.authorNeoh, K.G.
dc.contributor.authorKang, E.T.
dc.contributor.authorTan, K.L.
dc.date.accessioned2014-06-17T10:02:21Z
dc.date.available2014-06-17T10:02:21Z
dc.date.issued1994-01
dc.identifier.citationTing, Y.P., Neoh, K.G., Kang, E.T., Tan, K.L. (1994-01). Recovery of gold by electroless precipitation from acid solutions using polyaniline. Journal of Chemical Technology and Biotechnology 59 (1) : 31-36. ScholarBank@NUS Repository. https://doi.org/10.1002/jctb.280590106
dc.identifier.issn02682575
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/67535
dc.description.abstractThe oxidation of the leucoemeraldine (LM) and emeraldine (EM) states of polyaniline (PAN) and the subsequent reprotonation and reduction of the nigraniline (NA) and pernigraniline (PNA) in acid gold solution were utilized for the spontaneous and sustained reduction of gold. The rate of Au reduction is strongly dependent on the intrinsic oxidation state of the polymer and the polymer surface area. The rate also increases with decreasing pH of the chloroauric solution to about pH ~ 1. X-ray photoelectron spectroscopic (XPS) results indicate that only elemental gold or Au(0) accumulates on the polymer surface. The N1s core-level spectra of the protonated and base form of EM films after Au reduction confirm that the intrinsic structure of the polymer remains intact. The process, however, is limited by the decreasing effective surface area of the polymer due to Au deposition. The results indicate that an LM film accumulated up to five times its own weight of Au (Au/monomer mole ratio > 2) before the recovery rate was significantly retarded.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1002/jctb.280590106
dc.sourceScopus
dc.subjectAcid solution
dc.subjectAu reduction
dc.subjectPolyaniline
dc.subjectRedox states
dc.subjectXPS
dc.typeArticle
dc.contributor.departmentCHEMICAL ENGINEERING
dc.contributor.departmentPHYSICS
dc.description.doi10.1002/jctb.280590106
dc.description.sourcetitleJournal of Chemical Technology and Biotechnology
dc.description.volume59
dc.description.issue1
dc.description.page31-36
dc.description.codenJCTBD
dc.identifier.isiutA1994MR54100005
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