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dc.contributor.authorManu Jose-
dc.contributor.authorManoj, P H-
dc.contributor.authorShukla, S-
dc.date.accessioned2016-04-13T06:45:34Z-
dc.date.available2016-04-13T06:45:34Z-
dc.date.issued2014-12-
dc.identifier.citationJournal of Environmental Chemical Engineering 2(4):1980-1988,Decen_US
dc.identifier.urihttp://hdl.handle.net/123456789/2262-
dc.description.abstractThe dye-adsorption capacity of various adsorbents has been traditionally determined via conducting the equilibrium dye-adsorption/desorption experiments. We demonstrate here a new method for precisely predicting the dye-adsorption capacity of hydrothermally processed semiconductor-oxide nanotubes, such as the hydrogen titanate, which involves the use of one-step dye-removal method of novel chemically-activated catalytic process conducted in the dark. The methylene blue (MB) dye-adsorption capacity of hydrogen titanate nanotubes has been determined to be 121 mg g 1 via the conventional method which is comparable with that (114 mg g 1) predicted via the one-step dye-removal method of novel chemically-activated catalytic process conducted in the dark. The equilibrium MB adsorption on the surface of hydrogen titanate nanotubes follows both the Langmuir and Freundlich isotherms and the pseudo-second-order kinetics at the initial solution-pH of 10 although the amount of surface-coverage by the MB dye supports only the Langmuir modelen_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectAdsorption;Advanced oxidation process;Hydrogen peroxide; Kinetics;Equilibrium isothermen_US
dc.titlePredicting dye-adsorption capacity of hydrogen titanate nanotubes via one-step dye-removal method of novel chemically-activated catalytic process conducted in darken_US
dc.typeArticleen_US
Appears in Collections:2014

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