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Thermal Characterization of Poly(Styrene Sulfonate)/Layered Double Hydroxide Nanocomposites

Published online by Cambridge University Press:  28 February 2024

Christopher O. Oriakhi
Affiliation:
Department of Chemistry and Center for Advanced Materials Research, Oregon State University, Corvallis, Oregon 97331
Isaac V. Farr
Affiliation:
Department of Chemistry and Center for Advanced Materials Research, Oregon State University, Corvallis, Oregon 97331
Michael M. Lerner
Affiliation:
Department of Chemistry and Center for Advanced Materials Research, Oregon State University, Corvallis, Oregon 97331

Abstract

Phase and morphological changes during thermolysis of Mg4Al2(OH)12CO3·nH2O and Zn6Al2(OH)16CO3·nH2O layered double hydroxides (LDH) and their nanocomposites with poly(styrene sulfonate) (PSS) are studied by X-ray powder diffraction (XRD), scanning and transmission electron micrography (SEM and TEM) and thermal analyses. Mg4Al2(OH)12CO3·nH2O and Mg2Al(OH)6[CH2CH(C6H4SO3)]·3H2O show comparable thermal stabilities: the layered structure is lost above 300 °C with the nucleation of the MgO phase at approximately 400 °C and the MgAl2O4 phase at approximately 800 °C Zn3Al(OH)8[CH2CH(C6H4SO3)]·nH2O undergoes complete oxidative pyrolysis of the polyanion by 500 °C. Crystalline oxide products are obtained at a temperature approximately 300 °C lower than that of thermolysis of Zn6Al2(OH)16CO3·nH2O. The SEM and TEM images show that the thermolysis of LDH carbonates produces dense aggregates containing microcrystalline particles, whereas Mg2Al(OH)6[CH2CH(C6H4SO3)]·3H2O forms a macroporous solid.

Type
Research Article
Copyright
Copyright © 1997, The Clay Minerals Society

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