RESUMO

With the objective of producing a material showing better conductive properties to be used as a support for electroactive species, a SiO(2)/SnO(2) mixed oxide was prepared. The procedure for SiO(2)/SnO(2) mixed oxide preparation using the sol-gel processing method, starting from tetraethylorthosilicate and SnI(4) as precursor reagents, is described. SiO(2)/SnO(2) with composition Sn=15.6 wt% and S(BET) = 525 m(2)g(-1), V(p)=0.28 mlg(-1), and D(p)= 1.5 nm, where S(BET), V(p) and D(p) are the specific surface area, the average pore volume, and the average pore diameter, respectively, was obtained. The X-ray photoelectron spectroscopy showed that the mixed oxide was thermally very stable for samples heat-treated at up to 1073 K. The Brønsted acid sites, probed with pyridine molecules for samples heat-treated at various temperatures, were chemically stable up to 473 K. Segregation of SnO(2) crystalline phase was observed at 1473 K but no crystalline phase was verified for SiO(2) at this temperature. The porous SiO(2)/SnO(2) matrix was used as base for Cu(II) immobilization and an electrode was developed for application in electrochemical detection of vitamin C in tablets.

Assuntos

Ácido Ascórbico/química , Cobre/química , Eletroquímica/métodos , Dióxido de Silício/química , Compostos de Estanho/química , Microanálise por Sonda Eletrônica , Temperatura Alta , Modelos Químicos , Transição de Fase , Silanos/química , Termogravimetria , Fatores de Tempo , Difração de Raios X

RESUMO

Cellulose/antimony(III) oxide composites, Cel/Sb(2)O(3), with oxide loadings of 1.7, 5.4, and 9.2 wt% were prepared by reacting the precursor SbCl(3) reagent with cellulose in dry ethanol solution. The reaction of the Lewis acid and the cellulose fibers occurred at the~amorphous domains of the biopolymer, increasing the crystallinity degree of the composite compared with that of the untreated cellulose. The scanning electron microscopy images and metal mapping for all samples showed that the oxide film layer uniformly covered the fiber surfaces with no detectable agglomerates of the oxide particles. The synchrotron X-ray diffraction patterns indicated that the antimony oxide film was obtained as a crystalline phase with orthorombic structure. The atomic ratios of O/Sb, determined by X-ray photoelectron spectroscopy, indicated that, for Cel/Sb(2)O(3) samples with 9.3 wt% loading, the fiber surface is nearly saturated by the oxide layer. The thermal stability of Cel/Sb(2)O(3) compared to that of untreated cellulose is practically unaffected. Copyright 2000 Academic Press.