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dc.contributor.advisorClearfield, Abraham
dc.creatorYang, Chao-Yeuh
dc.date.accessioned2020-09-02T21:04:05Z
dc.date.available2020-09-02T21:04:05Z
dc.date.issued1986
dc.identifier.urihttps://hdl.handle.net/1969.1/DISSERTATIONS-20225
dc.descriptionTypescript (photocopy).en
dc.description.abstractA series of alkyl and aryl diphosphonic acids in which the size of the alkyl and aryl group is systematically varied has been synthesized. The corresponding zirconium diphosphonates, mixed-component pillared zirconium phosphite/phosphate diphosphonates, mixed-component non-pillared zirconium phosphite phenyl phosphonates and their sulphonated derivatives have been prepared by various synthetic methods. An extensive study of the preparative conditions of these synthetic methods has been carried out. The mixed-component pillared zirconium phosphate diphosphonates have zeolite-type cavities, exchangeable hydrogen ions, large surface area and high void volume, thus they constitute a new series of adsorbents for chromatography, new composite ion-exchangers and also new catalyst systems. These compounds were characterized by X-ray diffraction, TG analysis, elemental analysis, IR spectroscopy, titration curves, surface area measurement, pore size distribution, solid state NMR and electron microscopic study. Their various possible applications were also investigated. A series of layered zirconium phosphite phenylphosphonate and phosphate phenylphosphonate mixed derivatives, with the general formula Zr(XPO₃)[subscript 2-y](C₆H₅PO₃)[subscript y] (x = -H, -OH and y = 1.0-04), have been prepared and characterized. These compounds were readily sulfonated in fuming sulfuric acid under mild conditions and the resultant sulfonates behave as strong acid ion exchangers. These exchangers are colloidal in aqueous suspensions and exchange large cations and complexes in a facile manner. The exchanger showed increased selectivity for larger cations. In the case of coordination complexes the increased selectivity was remarkable and may stem from a combination of favorable electrostatic and steric factors. ...en
dc.format.extentxv, 182 leavesen
dc.format.mediumelectronicen
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.rightsThis thesis was part of a retrospective digitization project authorized by the Texas A&M University Libraries. Copyright remains vested with the author(s). It is the user's responsibility to secure permission from the copyright holder(s) for re-use of the work beyond the provision of Fair Use.en
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/
dc.subjectMajor chemistryen
dc.subject.classification1986 Dissertation Y22
dc.subject.lcshZirconium phosphateen
dc.subject.lcshDerivativesen
dc.titleOrgano-derivatives of zirconium phosphateen
dc.typeThesisen
thesis.degree.disciplineChemistryen
thesis.degree.grantorTexas A&M Universityen
thesis.degree.nameDoctor of Philosophyen
thesis.degree.namePh. D. in Chemistryen
thesis.degree.levelDoctorialen
dc.contributor.committeeMemberAnthony, R. G.
dc.contributor.committeeMemberDarensbourg, Donald J.
dc.contributor.committeeMemberMartell, A. E.
dc.contributor.committeeMemberRosynek, M. P.
dc.type.genredissertationsen
dc.type.materialtexten
dc.format.digitalOriginreformatted digitalen
dc.publisher.digitalTexas A&M University. Libraries
dc.identifier.oclc17860936


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