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Effect of Processing Variables on the Structural Evolution of Silica Gels
Authors:E. Drabarek  J. R. Bartlett  H. J. M. Hanley  J. L. Woolfrey  C. D. Muzny
Affiliation:(1) Materials Division, Australian Nuclear Science and Technology Organization, Private Mail Bag 1, Menai, NSW, 2234, Australia;(2) Physical and Chemical Properties Division, National Institute of Standards and Technology, Boulder, Colorado, 80303, U.S.A.;(3) Australian Nuclear Science and Technology Organization, Private Mail Bag 1, Menai, NSW, 2234, Australia
Abstract:Constant shear rate and dynamic rheological measurements have been used to investigate the effect of shear on the processes controlling the structural evolution (size and volume fraction of clusters and the extent of cluster–cluster cross-linking) during the gelation of colloidal silica sols. In the absence of shear, the storage and loss moduli (Gprime and GPrime, respectively) initially increase slowly prior to gelation, indicating that cluster growth and network formation are initially proceeding slowly, but then the system evolves rapidly, with cluster growth occurring at a slightly faster rate than network formation. In contrast, sols presheared for 4 h prior to gelation exhibit rapid increases in both Gprime and GPrime immediately after cessation of the applied shear, reflecting significant differences in the evolution of the gel structure. On aging, the viscoelastic properties of the unsheared and presheared samples are similar, indicating that their structures are comparable on the length scales (several microns) being probed by the frequency range used here. However, their chemical and microstructural properties differ significantly, due to differences in the intercluster bonds. The effect of shear rate, initial pH, colloid particle size, and volume fraction on the structure of the resulting sols and gels is discussed.
Keywords:gelation mechanism  gel point  gel structure  restructuring  rheology  silica  viscosity  viscoelasticity
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