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Network models, silica surfaces

Besides specific surface area, silicas are also characterised by their porosity. Most of the silica s are made out of dense spherical amorphous particles linked together in a three dimensional network, this crosslinked network building up the porosity of the silica. Where the reactivity of diborane towards the silica surface has been profoundly investigated, little attention has been paid to the effect of those reactions on the pore structure. However different methods are developed to define the porosity and physisorption measurements to characterise the porosity parameters are well established. Adsorption isotherms give the specific surface area using the BET model, while the analysis desorption hysteresis yields the pore size distribution. [Pg.347]

A description of silica surfaces should not be made only in terms of hydroxyl groups without reference to the underlying atoms. Various experimental results suggest some local order on the surface, even though the bulk network is amorphous. The presence of typical sites on the atomic scale is all the more likely because constraints due to disorder should relax on a hydroxylated surface. Therefore, network and surface models based... [Pg.209]

In order to explain such an evolution, we propose a very simple model describing the evolution of the surface properties of a silica surface submitted to a controlled silylation process. To describe a silylated surface, we first distribute randomly the TMS grafts on a model surface made of a hexagonal bi-dimensional network of sites as previously proposed by Sindorf and Maciel [7]. Such a silylated surface corresponding to a 30 % surface coverage by the TMS groups is shown on Fig. 5. [Pg.779]

On this basis the porosity and surface composition of a number of silicas and zeolites were varied systematically to maximize retention of the isothizolinone structures. For the sake of clarity, data is represented here for only four silicas (Table 1) and three zeolites (Table 2). Silicas 1 and 3 differ in their pore dimensions, these being ca. 20 A and 180 A respectively. Silicas 2 and 4, their counterparts, have been calcined to optimise the number and distribution of isolated silanol sites. Zeolites 1 and 2 are the Na- and H- forms of zeolite-Y respectively. Zeolite 3 is the H-Y zeolite after subjecting to steam calcination, thereby substantially increasing the proportion of Si Al in the structure. The minimum pore dimensions of these materials were around 15 A, selected on the basis that energy-minimized structures obtained by molecular modelling predict the widest dimension of the bulkiest biocide (OIT) to be ca. 13 A, thereby allowing entry to the pore network. [Pg.89]

Surface interactions between water and polymer networks have a profound effect on the water structure. The properties of water in these and other heterogeneous systems are sensitive to the size of the network pores and have been described by the two-phase model which assumes partition of the water between the "bulk and the "bound water phases" Evidence for this partition has been obtained in several proton NMR studies and also in ESR studies of paramagnetic probes in zeolites, silica gels and in water containing polymers. ... [Pg.266]


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See also in sourсe #XX -- [ Pg.211 ]




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