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Dissolution kinetics: The nature of the particle attack of layered silicates in HF

dc.contributor.authorKline, W. E.en_US
dc.contributor.authorFogler, H. Scotten_US
dc.date.accessioned2006-04-07T18:13:22Z
dc.date.available2006-04-07T18:13:22Z
dc.date.issued1981en_US
dc.identifier.citationKline, W. E., Fogler, H. S. (1981)."Dissolution kinetics: The nature of the particle attack of layered silicates in HF." Chemical Engineering Science 36(5): 871-884. <http://hdl.handle.net/2027.42/24574>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6TFK-443V58T-8C/2/15cf846a6933421f11c533fe282362eeen_US
dc.identifier.urihttps://hdl.handle.net/2027.42/24574
dc.description.abstractThe dissolution of layered silicates by hydrofluoric acid was studied with the aid of a slurry reactor. The nature of particle dissolution was delineat by measurements of reaction rates and by the examination of partially dissolved particles using a scanning electron microscope. The rates of particle d per unit mass were modeled as a function of the fraction x dissolved by an equation of the form [-r(x)]/[-r(x = 0)] = (1 - x) n-1. For the three layer silicates the parameter n takes on a value of 1/2, reflecting radial attack at the unit cell edges. The reactive edge surface area is considerably smaller than the total wetted particle surface area. In contrast, the two layer kaolinite structure dissolves at both the layer edges and the planar faces, and the parameter n varies from 0 to 1 as the particle dissolution proceeds to completion. Comparison of the rates of dissolution on the basis of the actual reactive surface areas show that layered silicates having the same octahedral sheet dissolve at the same rate. It is concluded that attack is preferential at surfaces where the octahedral sheets are exposed.en_US
dc.format.extent1125089 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleDissolution kinetics: The nature of the particle attack of layered silicates in HFen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelChemical Engineeringen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Chemical Engineering, The University of Michigan, Ann Arbor, MI 48109, U.S.A.en_US
dc.contributor.affiliationumDepartment of Chemical Engineering, The University of Michigan, Ann Arbor, MI 48109, U.S.A.en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/24574/1/0000857.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0009-2509(81)85041-5en_US
dc.identifier.sourceChemical Engineering Scienceen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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