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dc.creatorDoula, M. K.en
dc.creatorDimirkou, A.en
dc.date.accessioned2015-11-23T10:25:53Z
dc.date.available2015-11-23T10:25:53Z
dc.date.issued2008
dc.identifier10.1007/s10934-007-9102-x
dc.identifier.issn1380-2224
dc.identifier.urihttp://hdl.handle.net/11615/27197
dc.description.abstractThe concentration and the type of Cu2+ species adsorbed on a natural zeolite (Clinoptilolite) was measured and studied by using Electron Paramagnetic Resonance Spectroscopy (EPR). The EPR results together with macroscopic sorption data indicate that the solution ionic strength as well as, the type of electrolyte anion (Cl-, NO3- and SO42- ions were examined) affect the amount of Cu adsorbed and the type of Cu surface complexes. The increasing in solution pH affects Cu adsorption quantitatively whereas; the type of surface complexes formed depends mainly on solution ionic strength. For low solution ionic strength, when the inhibition from solution species is limited, the adsorbed Cu is characterized by more than one type of chemical environment. On the contrary, for high solution ionic strength the Cu adsorption is inhomogeneous and EPR spectra show only one type of surface complex. When the anions of the background electrolytes are different, but of equal normality, the results indicate that in the presence of SO42- discernible Cu surface complexes are formed whereas, for Cl- and NO3- these surface formations are obtained only for high Cu adsorbed concentrations.en
dc.source.uri<Go to ISI>://WOS:000256472500011
dc.subjectclinoptiloliteen
dc.subjectCu adsorptionen
dc.subjectEPRen
dc.subjectligandsen
dc.subjectsurface complexationen
dc.subjectELECTRON-PARAMAGNETIC-RESONANCEen
dc.subjectZEOLITESen
dc.subjectHYDROXIDEen
dc.subjectSURFACESen
dc.subjectCOPPERen
dc.subjectMONTMORILLONITEen
dc.subjectMECHANISMen
dc.subjectOXIDATIONen
dc.subjectCU-ZSM-5en
dc.subjectELEMENTSen
dc.subjectChemistry, Applieden
dc.subjectChemistry, Physicalen
dc.subjectMaterials Science,en
dc.subjectMultidisciplinaryen
dc.titleAn EPR study of Cu adsorption by clinoptilolite from Cl-, NO3 and SO42- solutionsen
dc.typejournalArticleen


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