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MODIFIED POLYACRYLONITRILE FOR ADSORPTION APPLICATIONS

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dc.contributor.author SIMITZIS, J en
dc.date.accessioned 2014-03-01T01:42:53Z
dc.date.available 2014-03-01T01:42:53Z
dc.date.issued 1994 en
dc.identifier.issn 0323-7648 en
dc.identifier.uri https://dspace.lib.ntua.gr/xmlui/handle/123456789/23970
dc.subject.classification Polymer Science en
dc.subject.other ACRYLAMIDE en
dc.title MODIFIED POLYACRYLONITRILE FOR ADSORPTION APPLICATIONS en
heal.type journalArticle en
heal.language English en
heal.publicationDate 1994 en
heal.abstract Polyacrylonitrile (PAN) was produced by redox polymerization of acrylonitrile and then was modified with 50% aqueous solutions of H2SO4 or NaOH. Copolymers of acrylonitrile' with acrylic acid, acrylamide or methylenebisacrylamide were prepared by radical polymerization. The structures of these polymers based on PAN were studied by IR-spectroscopy in order to determine their characteristic groups. The cation exchange capacity is higher in polymers containing more acidic groups (COOH), and for the examined cases the adsorbability was Cu2+ > Zn2+ (ion exchange selectivity). The discoloring ability of the examined polymers was studied with aqueous solutions of three dyes, i.e. methylene blue (cationic or basic dye), congo red (direct dye having similarities with anionic dyes) and alizarin yellow (acid dye or anionic monoazo dye). The results are interpreted in terms of electron donor-acceptor (EDA) interactions between the main groups of the polymers and the dyes. The presence of -CONH2 (having polar character) in the polymers based on PAN, produces favorable interactions with the groups (electron donor or acceptor) of the molecules of the three dyes. The design of new polymer materials based on PAN with increased adsorption ability, could be performed with such a discoloring investigation, especially for methylene blue and alizarin yellow. en
heal.publisher VCH PUBLISHERS INC en
heal.journalName ACTA POLYMERICA en
dc.identifier.isi ISI:A1994NK36800008 en
dc.identifier.volume 45 en
dc.identifier.issue 2 en
dc.identifier.spage 104 en
dc.identifier.epage 109 en


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